WO2013124286A1

WO2013124286A1 - Novel neurokinin 1 receptor antagonist compounds

Info

Publication number: WO2013124286A1
Application number: PCT/EP2013/053319
Authority: WO
Inventors: Morten Dahl SØRENSEN; Romani DI FABIO; Alfonso Pozzan; Maria Pia Catalani; Haakon BLADH; Jakob Felding
Original assignee: Leo Pharma A/S
Priority date: 2012-02-22
Filing date: 2013-02-20
Publication date: 2013-08-29
Also published as: JP6111274B2; CN104245702B; TW201339161A; CN104245702A; RU2014138032A; ES2568909T3; PL2817312T3; EP2817312B1; SG11201404880UA; US20150018345A1; RU2631319C2; EP2817312A1; HK1205104A1; JP2015511240A; KR20140122764A; MX2014010012A; AU2013224181A1; DK2817312T3; US9181259B2; CA2864440A1

Abstract

The present invention relates to a compound according to formula (A) wherein n is 1 or 2; R1 and R2 are independently hydrogen, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 alkoxy, CD3 or halogen; R3 is hydrogen, C(=O)OR7 or C_1-4 alkyl optionally substituted with hydroxy or NR8R9; R4 is hydrogen or oxo; R5 and R6 are independently hydrogen, hydroxy, NR8R9, C( =O)R7, C( =O)OR7, C( =O)NR8R9, C_1-4 alkyl, wherein said C_1-4alkyl is optionally substituted with hydroxy, NR8R9 or a 5- or 6-membered heterocyclic ring, wherein said 5- or 6-membered heterocyclic ring is optionally substituted with C_1-4 alkyl or C(=O)R7; or R5 and R6, together with the carbon atom to which they are attached, form =CH₂ or a 5- or 6-membered heterocycloalkyl, wherein said heterocycloalkyl is optionally substituted with C_1-4 alkyl; R7 is hydrogen or C_1-4 alkyl; R8 and R9 are independently hydrogen or C_1-4 alkyl, or R8 and R9, together with the nitrogen atom to which they are attached, form a 5- or 6-membered heterocyclic ring, or a pharmaceutically acceptable salt or solvate thereof. The invention relates further to intermediates for the preparation of said compounds, to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating or ameliorating pruritic dermal diseases or conditions with said compounds, and to the use of said compounds in the manufacture of medicaments.

Description

NOVEL NEUROKININ 1 RECEPTOR ANTAGONIST COMPOUNDS FIELD OF INVENTION The present invention relates to novel heterocyclic compounds which are neurokinin 1 receptor antagonists, to intermediates for the preparation of said compounds, to their use in therapy such as in the prophylaxis or treatment of pruritic dermal diseases or conditions, and to pharmaceutical compositions comprising said compounds. BACKGROUND OF THE INVENTION

Pruritus is a common symptom of skin diseases as well as a sign of an underlying systemic pathology. Pruritus is an unpleasant sensation in the skin that provokes a desire to scracth and may be acute (of short duration) such as the reaction to an insect bite or chronic (lasting for more than 6 weeks) such as in many inflammatory skin diseases. It is well known that patients with inflammatory skin diseases perceive pruritus as seriously compromising their quality of life.

Pruritus is mediated via free nerve endings of non-myelinated C-type nerve fibres in epidermis. These have been found to express neuropeptides, and the epidermal keratinocytes produce neuropeptides, receptors for neuropeptides, nerve growth factor, vanilloid receptors proteinase-activated receptor type 2 (PAR2) and voltage-gated ATP channels (MW Greaves, Curr. Allergy Asthma Rep. 10, 2010, pp. 236-242).

Neuropeptides suchs as Substance P have been shown to increase the production and release of nerve growth factor from cultured keratinocytes, suggesting that interactions between the immune system and the nervous system are important in the development of inflammation including pruritus. Inflammatory skin diseases such as atopic dermatitis, contact dermatitis, psoriasis and urticaria are associated with increased production of cytokines, neurotrophins and neuropeptides that may exacerbate the pruritus (U. Raap et al., Curr. Opin. Allergy Clin. Immunol. 11, 2011, pp. 420-427). While neuropeptides such as Substance P are not considered crucial for the pathogenesis of inflammatory skin diseases such as atopic dermatitis, they do play an important role in the development and severity of the condition, for instance by provoking the itch-scratch cycle where scratching exacerbates the inflammatory symptoms of atopic dermatitis (J. Salomon and E. Baran, JEADV 22, 2008, pp. 223-228). Furthermore, an increase of dermal nerves and upregulation of receptors for neuropeptides, e.g. the neurokinin 1 receptor has been found in skin from psoriasis patients with pruritus as opposed to skin from psoriasis patients without pruritus (S-E. Chang et al., Br. J. Dermatol. 156, 2007, pp. 1272- 1277).

It has also been found that other cell types resident in skin release mediators of pruritus. Thus, mast cells contain large amounts of histamine that are released on activation of the cells and induce pruritus by targeting histamine H I receptors on nerve endings. Eosinophils which infiltrate inflamed skin in atopic dermatitis, urticaria and contact dermatitis produce and release neurotrophins such as nerve growth factor. Current therapeutic treatments of pruritus include both topical and systemic

medicaments. Topical treatments include emollients and barrier creams that are believed to act by improving the barrier function of the skin, corticosteroids that do not appear to be antipruritic in themselves but act by relieving the attendant skin inflammation. This may also be the case for calcineurin inhibitors such as tacrolimus which has been shown to reduce pruritus in atopic dermatitis patients. Histamine HI antagonists have also shown effect against pruritus in atopic dermatitis patients, but exhibits systemic side effects in the form of drowsiness in a significant number of patients. Local anesthetics such as lidocain have been found to exhibit anti-pruritic properties (Patel and

Yosipovitch, Expert. Opin. Pharmacother. 11 (10), 2010, 1673-1682).

Systemic therapy of pruritus include oral antihistamines, antidepressants, neuroleptics and immunosuppressants such as cyclosporin. A neurokinin-1 receptor antagonist, aprepitant, which has been developed as an oral antiemetic drug for use to counteract the nausea and vomiting caused by chemotherapy or post surgery, has been found to relieve pruritus in patients suffering from Sezary syndrome by oral administration (Duval and Dubertret, New Engl. J. Med. 361 , 2009, pp. 1415-1416) and in patients with atopic diathesis, prurigo nodularis and systemic pruritus (S. Stander et al., Plos One, 2010, p. 5). WO01/25219 discloses piperazine derivatives which are antagonists of tachykinins, including substance P and other neurokinins.

WO02/32867 discloses piperidine derivatives which are antagonists of tachykinins, including substance P and other neurokinins

WO02/081457 discloses 1,4-diazepane-l-carboxylic acid derivatives process for their preparation and their use as tachykinin antagonists WO2009002770 discloses 6.5 pyrrolopiperidine tachykinin receptor antagonists.

As many of the antipruritic treatments available at present have side-effects that may limit their use, and as many dermal conditions are preferentially treated with topical medications, especially when the conditions is of mild to moderate severity, there is a continued need to develop neurokinin 1 receptor (NKIR) antagonists which are effective in the treatment of itch on topical application, but which have reduced systemic effects on the central nervous system.

SUMMARY OF THE INVENTION

In one aspect, the present invention relates to compounds of general formula A

A

wherein

n is 1 or 2;

Rl and R2 are independently hydrogen, Ci_-4 alkyl, Ci_-4 haloalkyl, Ci_-4 alkoxy, CD₃ or halogen;

R3 is hydrogen, C(=0)OR7 or Ci_-4 alkyl optionally substituted with hydroxy or NR8R9; R4 is hydrogen or oxo;

R5 and R6 are independently hydrogen, hydroxy, NR8R9, C(=0)R7, C(=0)OR7, C(=0)NR8R9, Ci-4 alkyl, wherein said Ci_-4 alkyl is optionally substituted with hydroxy, NR8R9 or a 5- or 6-membered heterocyclic ring, wherein said 5- or 6-membered heterocyclic ring is optionally substituted with Ci_-4 alkyl or C(=0)R7; or R5 and R6, together with the carbon atom to which they are attached, form =CH₂ or a 5- or 6- membered lieterocycloalkyi, wherein said lieterocycloalkyi is optionally substituted with Ci-4 alkyl;

R7 is hydrogen or Ci_-4 alkyl; R8 and R9 are independently hydrogen or Ci_-4 alkyl, or R8 and R9, together with the nitrogen atom to which they are attached, form a 5- or 6-membered heterocyclic ring, or a pharmaceutically acceptable salt or solvate thereof.

In another aspect, the present invention relates to a compound according to general formula A for use in therapy.

In another aspect, the present invention relates to a compound according to general formula A for use in the prevention, treatment or amelioration of pruritic skin conditions, e.g. acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurological or psychosomatic/psychiatric origin, including endocrine and metabolicdisorders, infections, haematological and

lymphoproliferative diseases, solid neoplasms and drug-induced pruritus; mastocytosis; pruritus of unknown cause; pruritus with chronic secondary scratch lesions, such as prurigo nodularis, and all types of prurigo; or any other dermal disease or condition characterized by pruritus.

In another aspect, the present invention relates to a pharmaceutical composition comprising, as a therapeutically active ingredient, a compound according to general formula A and a pharmaceutically acceptable carrier or vehicle.

In another aspect, the present invention relates to intermediates for the preparation of a compound according to general formula A, such as a compound according to general formula B,

B

wherein RIO is selected from the group consisting of hydrogen and -C(0)OCi-C₄ alkyl ; Rl l is selected from the group consisting of hydrogen and oxo;

R12 and R13 are independently selected from the group consisting of hydrogen, Ci-C₄ alkyl, allyl and -C(0)0(d-C₄ alkyl) ;

R14 is selected from the group consisting of Ci-C₄ alkyl ;

n is 1 or 2;

or a pharmaceutically acceptable salt thereof.

The compounds of formula A have been found to act as potent antagonists of NKIR and are therefore potentially useful in the treatment of any disease or condition where Substance P is involved in the disease pathology, in particular in the prevention, treatment or amelioration of a pruritic dermal disease or condition.

It has been found that some compounds of general formula A attenuate NK- 1 agonist induced scratching in the gerbil upon topical pre-treatment with said compounds.

It has surprisingly been found that some compounds of formula A exhibit a high metabolic clearance, i .e. are quickly degraded upon systemic administration, which makes them uniquely suitable for topical application with a favourable safety profile.

It has surprisingly been found that some compounds of general formula A exhibit a favourable ratio between the in vitro efficacy of the compound and the in vitro efficacy of metabolites of the compound, thus providing a favourable safety profile of the

compounds. It has surprisingly been found that some compounds of general formula A exhibit a mode of action indicating a competitive, non-surmountable antagonism, suggesting a slow dissociating antagonist-receptor complex. It has surprisingly been found that some compounds of general formula A both exhibit a mode of action indicating a competitive, non-surmountable antagonism as well as exhibiting a favourable ratio between the in vitro efficacy of the compound and the in vitro efficacy of metabolites of the compound. BRIEF DESCRIPTION OF THE DRAWINGS

Figure 1 is a graph showing the time course of scratching after a topical application of Compound 9 and Compound 44 in the NK-1 agonist-induced scratching model in the gerbil. The X-axis shows the time (minutes). The Y-axis shows the number of scratches (counts).

Figure la shows the effect of a topical application of Compound 9 and Compound 44 (dose 1%) in the first 10 minutes observation time of scratching model. The X-axis shows the compounds. The Y-axis shows the number of scratches (counts).

Figure 2 is a graph showing the time course of scratching after a topical application of Compound 60 and Compound 54 in the NK-1 agonist-induced scratching model in the gerbil. The X-axis shows the time (minutes). The Y-axis shows the number of scratches (counts).

Figure 2a shows the effect of a topical application of Compound 60 and Compound 54 (dose 1%) in the first 10 minutes observation time of scratching model. The X-axis shows the compounds. The Y-axis shows the number of scratches (counts). Figure 3 is a graph showing the time course of scratching after a topical application of Compound 38 and Compound 55 in the NK-1 agonist-induced scratching model in the gerbil. The X-axis shows the time (minutes). The Y-axis shows the number of scratches (counts). Figure 3a shows the effect of a topical application of Compound 38 and Compound 55 (dose 1%) in the first 10 minutes observation time of scratching model. The X-axis shows the compounds. The Y-axis shows the number of scratches (counts). DETAILED DESCRIPTION OF THE INVENTION Definitions

The term "alkyl" is intended to indicate a radical obtained when one hydrogen atom is removed from a hydrocarbon. Said alkyl may be branched or straight and may comprise 1-20, preferably 1-12, such as 1-6, such as 1-4 carbon atoms, such as 1-3 carbon atoms, such as 1-2 carbon atoms, such as 2-3 carbon atoms,. The term includes the subclasses normal alkyl (/7-alkyl), secondary and tertiary alkyl, such as methyl, ethyl, n- propyl, isopropyl, /7-butyl, isobutyl, sec-butyl, tert.-butyl, pentyl, isopentyl, neopentyl and hexyl. The term "cycloalkyl" is intended to indicate a saturated cycloalkane hydrocarbon radical, comprising 3-6 carbon atoms, such as 3-5 carbon atoms, such as 5-6 carbon atoms or such as 3-4 carbon atoms, e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. The term "heterocyclic ring" is intended to indicate radicals of 5- or 6-membered heterocyclic aromatic rings (also termed "heteroaryl") with 1-4 heteroatoms selected from 0, S and N, e.g. pyridyl, quinolyl, isoquinolyl, indolyl, dihydroisoindolyl, tetrazolyl, thiazolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thienyl, pyrazinyl, pyridazinyl, isothiazolyl, or heterocycloalkyl with 1-4 heteroatoms selected from 0, S and N, e.g. piperidinyl, piperazinyl, morpholinyl, pyrrolidinyl, tetrahydropyranyl,

tetrahydrothiopyranyl, thiane-l-oxid or thiane-l-dioxid or tetrahydrofuranyl,.

The term "halogen" is intended to indicate a substituent from the 7^th main group of the periodic table, such as fluoro, chloro, bromo and iodo.

The term "haloalkyl" is intended to indicate an alkyl radical as defined above substituted with one or more halogen atoms, e.g trifluoromethyl, difluoromethyl or fluoromethyl.

The term "heterocycloalkyl" is intended to indicate a cycloalkyl as described herein, wherein one or more carbon atoms are replaced by heteroatoms, comprising 1-5 carbon atoms, e.g. 2-5 or 2-4 carbon atoms, further comprising 1-4 heteroatoms, preferably 1, 2, or 3 heteroatoms, such as 1 or 2 heteroatoms, selected from 0, N, or S. The term "hydroxyalkyl" is intended to indicate an alkyl group as defined above substituted with one or more hydroxy, e.g. hydroxymethyl, hydroxyethyl,

hydroxypropyl.

The term "alkoxy" is intended to indicate a radical of the formula -OR', wherein R' is alkyl as indicated above, e.g. methoxy, ethoxy, n-propoxy, isopropoxy, butoxy, etc.

The term "oxo" is intended to indicate an oxygen atom which is connected to a carbon atom by a double bond, thereby forming a carbonyl group together with the carbon- atom to which it is connected.

The term "pharmaceutically acceptable salt" is intended to indicate salts prepared by reacting a compound of formula A or B with a suitable inorganic or organic acid, such as hydrochloric, hydrobromic, hydroiodic, sulfuric, nitric, phosphoric, formic, acetic, 2,2- dichloroaetic, adipic, ascorbic, L-aspartic, L-glutamic, galactaric, lactic, maleic, L-malic, phthalic, citric, propionic, benzoic, glutaric, gluconic, D-glucuronic, methanesulfonic, salicylic, succinic, malonic, tartaric, benzenesulfonic, ethane-l,2-disulfonic, 2-hydroxy ethanesulfonic acid, toluenesulfonic, sulfamic or fumaric acid.

The term "solvate" is intended to indicate a species formed by interaction between a compound, e.g. a compound of formula A, and a solvent, e.g . alcohol, glycerol or water, wherein said species are in a solid form. When water is the solvent, said species is referred to as a hydrate.

The term 'non-surmountable antagonist' or 'insurmountable antagonist' is intended to indicate an antagonist which produces shifts to the right of agonist concentration- response curves in the presence of increasing antagonist concentrations with depression of the maximal response to the agonist (ref. Kenakin, T. et. al., J. Pharm. Exp. Ther., (2006), 319, p. 710-723).

The term 'surmountable antagonist' is intended to indicate an antagonist which produces shifts to the right of agonist concentration-response curves in the presence of increasing antagonist concentrations with no concomitant diminution of the maximal response to the agonist, (ref. Kenakin, T. et. al., J. Pharm. Exp. Ther., (2006), 319, p. 710-723). Chronic pruritus on diseased skin is intended to indicate pruritus in skin diseases which are accompanied by itch, such as inflammatory, infectious, or autoimmune

cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas.

Genodermatoses are intended to include Darier's disease, Hailey-Hailey disease, ichthyoses, Sjogren-Larsson syndrome, EB pruriginosa .

Dermatoses of pregnancy are intended to include polymorphic eruption of pregnancy, pemphigoid gestationis, prurigo gestationis.

Skin lymphomas are intended to include cutaneous T-cell-lymphoma, cutaneous B- celllymphoma . Pruritic diseases of systemic origin are intended to comprise diseases arising from diseases of organs other than the skin, such as liver, e.g. primary biliary cirrhosis;

kidney,e.g. chronic renal failure; blood, e.g.Hodgkin's disease; and certain multifactorial, e.g. metabolic states or drugs. Pruritic systemic endocrine and metabolic diseases are intended to comprise chronic renal failure, liver diseases with or without cholestasis, hyperthyroidism, malabsorption, perimenopausal pruritus.

Pruritic systemic infectious diseases are intended to comprise HIV-infection,

helminthosis, Parasitosis.

Pruritic systemic haematological and lymphoproliferative diseases are intended to comprise iron deficiency, polycythaemia vera, Hodgkin's disease, Non-Hodgkin's lymphoma, plasmocytoma.

Chronic secondary scratch lesions are intended to indicate secondary acquired lesions induced by chronic scratching, such as for example lichen simplex chronicus, lichen Vidal, lichen amyloidosus, macular amyloidosus, and prurigo nodularis. Embodiments of the present invention

In an embodiment the present invention relates to compounds of general formula A, wherein

n is 1 or 2;

Rl and R2 are independently hydrogen, Ci_-4 alkyl, Ci_-4 haloalkyl, Ci_-4 alkoxy or halogen; R3 is hydrogen, C(=0)OR7 or Ci_-4 alkyl optionally substituted with hydroxy or NR8R9; R4 is hydrogen or oxo;

R5 and R6 are independently hydrogen, hydroxy, NR8R9, C(=0)R7, C(=0)OR7,

C(=0)NR8R9, Ci_-4 alkyl optionally substituted with hydroxy, NR8R9 or a 5- or 6- membered heterocyclic ring optionally substituted with Ci_-4 alkyl or C(=0)R7, or R5 and R6, together with the carbon atom to which they are attached, form =CH₂ or a 5- or 6- membered heterocyclic ring optionally substituted with Ci_-4 alkyl;

R7 is hydrogen or Ci_-4 alkyl;

R8 and R9 are independently hydrogen or Ci_-4 alkyl, or N8 and R9, together with the nitrogen atom to which they are attached, form a 5- or 6-membered heterocyclic ring, or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment, n in general formula A is 1.

In an embodiment, R4 is oxo.

In an embodiment, R4 is hydrogen.

In an embodiment, R3 is hydrogen, CH₃, CH₂OH, CH₂CH₂OH, COOCH₃ or CH₂N(CH₃)₂.

In an embodiment, R5 and R6 are both hydrogen. In an embodiment, R5 is hydrogen, CH₃, CH₂OH or CH₂CH₂OH, and R6 is COOH,

COOCH₃, CH₂OH, CH₂CH₂OH, CON(CH₃)₂ or CH₂-morpholine, CH₂-pyrrolidine, CH₂- piperazine optionally N-substituted with acetyl, or CH₂-piperidine.

In an embodiment R5 is hydrogen, CH₃, CH₂OH or CH₂CH₂OH, and R6 is COOH, COOCH₃, CH₂OH, CH₂CH₂OH, CON(CH₃)₂ or CH₂-morpholine, CH₂-pyrrolidine, CH₂-piperazine optionally N-substituted with acetyl, or CH₂-piperidine.

In an embodiment, R5 and R6, together with the carbon atom to which they are attached form a piperidine ring optionally substituted with Ci_-4 alkyl.

In an embodiment, R5 and R6, together with the carbon atom to which they are attached form =CH₂, a piperidine ring optionally substituted with Ci_-4 alkyl, or a tetrahyd ropy ran ring. In an embodiment, the compound is one of general formula A(iii)

A(iii)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated above,

or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment, Rl is hydrogen, CH₃, fluoro or trifluoromethyl.

In an embodiment, R2 is hydrogen, CH₃ or trifluoromethyl.

In an embodiment, R2 is hydrogen, chloro, CH₃, CH₂CH₃, isopropyl, OCH₃, difluoromethyl or trifluoromethyl.

In an embodiment, Rl and R2 are both trifluoromethyl.

In an embodiment, Rl is trifluoromethyl and R2 is methyl, ethyl or isopropyl.

Specific examples of compounds of the invention are selected from the group consisting of

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2- a]piperazine-2-ca rboxamide

N- [(3, 5-dimethyl phenyl) methyl] -N-methyl- l-(2-methyl pheny l)-6-oxo- ctahydropyrrolo[ l,2- a]piperazine-2-ca rboxamide

N-{ [3-fluoro-5-(trifluoromethyl) phenyl] methyl }-N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide

N-{ [3-fluoro-5-(trifluoromethyl) phenyl] methyl }-N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide N-methyl- l-(2-methy I phenyl)-6-oxo-N-{[3-(trifluoromethy I) phenyl] methyl }- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

N-methyl- l-(2-methy I phenyl)-6-oxo-N-{[3-(trifluoromethy I) phenyl] methyl }- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7-oxo- octahydro-lH-pyrrolo[ l,2-a] [ l,4]diazepine-2-carboxamide

2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carba moyl)-7-methyl-l -(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-7-carboxylic acid

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine 2 carboxamide

Methyl 2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carbamoyl)-7-methy I- 1-(2- methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a}piperazine-7-carboxylate

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide

2-N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-2-N,7-N,7-N,7-tetramethyl- l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2,7-dicarboxamide

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide methanesulfonic acid salt

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7- (morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-6-oxo-7- (pyrrolidin-l-ylmethyl)-octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-ethyl- l-(2-methyl pheny l)-6-oxo-7-

(pyrrol id in-l-ylmethyl)-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N-methyl-7-methylidene-l-(2- methy I pheny l)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide

N-{ 1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethy l)-N-methyl- l-(2-methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a]piperazine-2-ca rboxamide

N-{ 1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethy l)-N-methyl- l-(2- methy I pheny l)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide

7- [(4-acetylpiperazin-l-yl) methyl] -N-{ [3, 5-bis(trifluoromethyl)phenyl] methyl }-N- methyl-l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide N-{ [3,4-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7- (morpholin-4-ylmethyl)-6-oxa-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide as methansulfonic acid salt N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7- (morpholin-4-ylmethyl)-6-oxa-octahyd ropyrrolo[ l,2-a] piperazine-2-carboxamide methansulfonic acid salt

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7- (morpholin-4-ylmethyl)-6-oxa-octahyd ropyrrolo[ l,2-a] piperazine-2-carboxamide methansulfonic acid salt

N-{[3,5-bis(trifluoromethyl)phenyl] methyl}-7,7-bis(2-hydroxyethyl)-N-methyl- l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a] piperazine-2-carboxamide

(3'aS,4'S)-N-{ [3,5-bis(trifluoromethyl)phenyl]methyl}-N, l-dimethyl-4'-(2- methyl phenyl)- 1 '-oxo-hexahyd ro- l 'H-spiro[ pi peridine-4,2'-pyrrolo[ l,2-a] pi perazine] -5'- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N, l-di methyl-4'-(2-methyl phenyl)- 1 '-oxo- hexahydro- l'H-spiro[piperidine-4,2'-pyrrolo[ l,2-a] piperazine]-5'-ca rboxamide

N-{[3,5-bis(trifluoromethyl)phenyl] methyl}-7-(hydroxymethyl)-N-methyl- l-(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide

In an embodiment specific examples of compounds of the invention are selected from the group consisting of N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide,

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methyl phenyl)-6-oxo- ctahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-{[3-fluoro-5-(trifluoromethyl) phenyl] methyl }-N-methy 1- 1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide, N-{[3-fluoro-5-(trifluoromethyl) phenyl] methyl }-N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-methy 1-1 -(2-methylphenyl)-6-oxo-N-{[3-(trifluoromethyl)pheny I] methyl }- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

(lS,8aS)-N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a] piperazine-2-carboxamide,

(lR,8aR)-N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a] piperazine-2-carboxamide,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N-methyl-l-(2-methylphenyl)-7-oxo- octahydro-lH-pyrrolo[ l,2-a] [ l,4]diazepine-2-carboxamide,

2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carba moyl)-7-methyl-l -(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-7-carboxylic acid,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine 2 carboxamide,

Methyl 2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carbamoyl)-7-methy I- 1-(2 methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a}piperazine-7-carboxylate,

Methyl 2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carbamoyl)-7-methy I- 1-(2 methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a}piperazine-7-carboxylate ,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide, N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{[3,5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

2-N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-2-N,7-N,7-N,7-tetramethyl- l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2,7-dicarboxamide,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide methanesulfonic acic salt,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N-methyl-l-(2-methylphenyl)-7-(morphol

4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-6-oxo-7-

(pyrrol id in-l-ylmethyl)-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N-methyl-7-methylidene-l-(2- methy I pheny l)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-{ 1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethyl)-N-methyl l-(2-methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a]piperazine-2-ca rboxamide,

N-{1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethyl)-N-methyl l-(2-methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a]piperazine-2-ca rboxamide,

N-{1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethyl)-N-methyl l-(2-methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide, 7- [(4-acetylpiperazin-l-yl) methyl] -N-{ [3, 5-bis(trifluoromethyl)phenyl] methyl }-N- methyl-l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide, N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}-N-methyl-l-(2-methylphenyl)-7-(morpholin 4-ylmethyl)-6-oxa-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide as methansulfonic acid salt,

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}-N-methyl-l-(2-methylphenyl)-7-(morpholin 4-ylmethyl)-6-oxa-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide methansulfonic acid salt,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

(3'aS,4'S)-N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N,l-dimethyl-4'-(2- methylphenyl)-l'-oxo-hexahydro-l'H-spiro[piperidine-4,2'-pyrrolo[ l,2-a]piperazine]-5'- ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N,l-d imethyl-4'-(2-methyl phenyl)- 1 '-oxo- hexahydro-l'H-spiro[ pi peridine-4,2'-pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-N,l-d imethyl-4'-(2-methyl phenyl)- 1 '-oxo- hexahydro-l'H-spiro[ pi peridine-4,2'-pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-7-(hydroxymethyl)-N-methyl-l -(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l-

(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l-2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide , N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l (2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-{[3,5-bis(tnfluoromethyl)phenyl]methyl}-N-methyl-l-(2-methylphenyl)- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-{[3,5-bis(tnfluoromethyl)phenyl]methyl}-7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide, N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7- (morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide, /V-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-/V-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine 2 carboxamide ,

(lS,8aS)-/V-(3-fluoro-5-(tnfluoromethyl)benzyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-/V-(3-methyl-5-(tnfluoromethyl)benzyl)-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-(3-methoxy-5-(tnfluoromethyl)benzyl)-/V-methyl-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-(3-chloro-5-(trifluoromethyl)benzyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl-/V-(3- (trifluoromethyl) benzyl) hexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-(l-(3,5-bis(trifluoromethyl)phenyl)-3-hydroxypropyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-(l-(3,5-bis(trifluoromethyl)phenyl)propyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-/V-((S)-l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)- ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-/V-((R)-l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l H)- ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl-/V-((R)-l-(3- (trifluoromethy I) phenyl)ethyl)hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide, (lS,8aS)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)- /V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)- /V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide, (lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-methoxy-5-

(trifluoromethy I) phenyl)ethyl)-/V-methy 1-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l, 2- a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-l-(3-fluoro-5-(tnfluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-fluoro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methoxy-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl) /V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyloctahydro-l'/-/-spiro[pyran-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, (l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyloctahydro-l'/-/-spiro[pyran-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, (lS,8aS)-7-(hydroxymethyl)-/V-methyl-/V-((R)-l-(3-methyl-5-

(trifluoromethy I) phenyl)ethyl)-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- carboxamide ,

(lS,8aS)-7,7-bis(hydroxymethyl)-/V-methyl-/V-((R)-l-(3-methyl-5-

(trifluoromethy I) phenyl)ethyl)-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide, (lS,8aS)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)-/V- methy 1-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-/V,l-dimethyl-6'-oxo-l'-o- tolyltetrahydro-l'/-/-spiro[piperidine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-carboxamide, formic acid salt,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyltetrahydro-l'/-/-spiro[piperidine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-carboxamide, formic acid salt^

(lS,8aS)-/V-methyl-/V-((R)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)- /V-methyl-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl) -/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment specific examples of compounds of the invention are selected from the group consisting of

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l- (2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide ,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide , N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l- (2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l- (2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide ,

N-{ [3, 5-bis(tnfluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

/V-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-/V-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine 2 carboxamide ,

(lS,8aS)-/V-(3-fluoro-5-(trifluoromethyl)benzyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide, (lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-/V-(3-methyl-5-(tnfluoromethyl)benzyl)-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-(3-chloro-5-(tnfluoromethyl)benzyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl-/V-(3- (trifluoromethyl)benzyl)hexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl-/V-((R)-l-(3-

(trifluoromethy I) phenyl)ethyl)hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-

/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-methoxy-5-

(trifluoromethy I) phenyl)ethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l, 2- a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide, (lS,8aS)-/V-((R)-l-(3-fluoro-5-(tnfluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V methy 1-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((S)-l-(3-fluoro-5-(tnfluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methoxy-5-(tnfluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl) /V-methyl-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo- 1-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(trifluoromethy I) phenyl)ethyl)-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- carboxamide ,

(lS,8aS)-7,7-bis(hydroxymethyl)-/V-methyl-/V-((R)-l-(3-methyl-5-

(trifluoromethy I) phenyl)ethyl)-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)-/V- methyl-6-oxo- 1-o-toly I hexahyd ropy rrolo[l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V,l-dimethyl-6'-oxo-l'-o- tolyltetrahydro-l'/-/-spiro[ pi peridine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, formic acid salt, (l'S,8a'S)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyltetrahydro-l'H-spiro[pipendine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-carboxamide, formic acid salt,

(lS,8aS)-/V-methyl-/V-((R)-l-(3-methyl-5-(tnfluoromethyl)phenyl)ethyl)-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-chloro-5-(tnfluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)- /V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(tnfluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-/V-((R)-l-(3-isopropyl-5-(tnfluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl) -/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is N-[(1R)-1- [3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine-2-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)-N- [(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine-2-carboxamide, or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lR,8aR)-N- [(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine-2-carboxamide, or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is N-{[3,5- bis(trifluoromethyl)phenyl]methyl}-7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide or a

pharmaceutically acceptable salt or solvate thereof. In an embodiment of the invention the compound according to formula A is N-[(1R)-1- [3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l-2- methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide or a

pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is N-[(1R)-1- [3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)- 7,7-bis(2-hydroxyethyl)-/V-methyl-/V-((S)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)- 6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a

pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)- 7,7-bis(2-hydroxyethyl)-/V-methyl-/V-((R)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)- 6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a

pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)-/V- ((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)-/V- ((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)-/V-methyl-6-oxo- l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)-/V- ((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is (lS,8aS)-/V- ((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V-methyl-6- oxo-l-o-tolylhexahydropyrrolo[ l,2-a] pyrazine-2( l/-/)-ca rboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is ( lS,8aS)-/V- ((R)- l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo- l-o- tolylhexahydropyrrolo[ l,2-a] pyrazine-2( l/-/)-carboxamide or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment of the invention the compound according to formula A is ( lS,8aS)- 7,7-bis(2-hydroxyethyl)-/V-((R)- l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl) -N- methyl-6-oxo- l-o-tolylhexahyd ropyrrolo[ l,2-a] pyrazine-2( l/-/)-carboxamide

or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment Rl is Ci_-4 haloalkyl and R2 is Ci_-4 haloalkyl, Ci_₄ alkyl or halogen .

In an embodiment Rl is Ci_-4 haloalkyl and R2 is Ci_₄ alkyl. In an embodiment Rl a nd R2 are Ci_-4 haloalkyl . In an embodiment Rl is trifluoromethyl or difluoromethyl and R2 is Ci_-4 alkyl. In an embodiment Rl is trifluoromethyl and R2 is methyl, ethyl or isopropyl . In an embodiment R3 is Ci_-4 alkyl .

In an embodiment R3 is methyl .

In an embodiment R3 is Ci_₄ alkyl optionally substituted with hydroxy. In an embodiment n is 1 and R4 is oxo.

In an embodiment n is 1 and R4 is hydrogen. In an embodiment R5 a nd R6 are hydrogen .

In an embodiment R5 is hydrogen and R6 is Ci_₄ alkyl optionally substituted with hydroxy I . In an embodiment R5 a nd R6 are independantly Ci_₄ alkyl optiona lly substituted with hydroxy I . In an embodiment R5 a nd R6 are hydroxymethyl or hydroxyethyl . In an embodiment R5 a nd R6 are hydroxyethyl .

In an embodiment R5 a nd R6 together with the carbon atom to which they are attached, form a 5- or 6-membered heterocycloalkyi, wherein said heterocycloalkyi is optionally substituted with Ci_-4 alkyl .

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl and R3 is Ci_₄ alkyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl and R3 is Ci_₄ alkyl optionally substituted with hydroxy I.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and R5 and R6 are hydroxy-Ci-₄ alkyl.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl and R5 and R6 are hydroxy-Ci-₄ alkyl.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl and R5 and R6 are hydrogen

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl and R5 is hydrogen and R6 is Ci_₄ alkyl optionally substituted with hydroxyl.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl and R5 and R6 are independantly Ci_-4 alkyl optionally substituted with hydroxyl.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl and R4 is oxo.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl and R4 is hydrogen. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl and R5 and R6 together with the ca rbon atom to which they a re attached, form a 5- or 6-membered heterocycloalkyl, wherein said heterocycloalkyl is optionally substituted with Ci_-4 alkyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and n is 1. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R5 and R6 are hydroxy-Ci-₄ alkyl and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R5 and R6 are hydrogen and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl, R5 is hydrogen and R6 is Ci_₄ alkyl optionally substituted with hydroxyl and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl, R5 and R6 are independantly Ci_-4 alkyl optionally substituted with hydroxyl and n is 1. In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl, R5 and R6 together with the ca rbon atom to which they a re attached, form a 5- or 6-membered heterocycloalkyl, wherein said heterocycloalkyl is optionally substituted with Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl and R4 is oxo.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and R4 is oxo.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R4 is oxo and R5 and R6 are hyd roxy-Ci-₄ alkyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl, R4 is oxo and R5 and R6 are hydroxy-Ci-4 alkyl .

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_₄ alkyl, R4 is oxo and R5 and R6 are hydrogen.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R4 is oxo and R5 is hydrogen and R6 is Ci-4 alkyl optionally substituted with hydroxyl. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R4 is oxo and R5 and R6 are independantly Ci_-4 alkyl optionally substituted with hydroxyl .

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R4 is oxo and R5 and R6 together with the carbon atom to which they are attached, form a 5- or 6-membered

heterocycloalkyl, wherein said heterocycloalkyl is optionally substituted with Ci_-4 alkyl .

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a pha rmaceutically acceptable sa lt or solvate thereof.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a pha rmaceutically acceptable sa lt or solvate thereof. An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_-4 alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-₄ haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl, R3 is Ci_-4 alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R3 is Ci_-4 alkyl. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R3 is Ci_₄ alkyl optionally substituted with hydroxyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and R5 and R6 are hyd roxy-Ci_₄ alkyl .

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl and R5 and R6 are hydroxy-Ci_₄ alkyl .

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R5 and R6 are hydrogen

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R5 is hydrogen and R6 is Ci_₄ alkyl optionally substituted with hydroxyl.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R5 and R6 are independantly Ci_₄ alkyl optionally substituted with hydroxyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and n is 1.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl and R4 is oxo.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl and R4 is hydrogen.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl and R5 and R6 together with the ca rbon atom to which they are attached, form a 5- or 6-membered heterocycloalkyi, wherein said heterocycloalkyi is optionally substituted with Ci_₄ alkyl .

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and n is 1. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R5 and R6 are hydroxy-Ci_₄ alkyl and n is 1.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R5 and R6 are hydrogen and n is 1. In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R5 is hydrogen and R6 is Ci_₄ alkyl optionally substituted with hydroxyl and n is 1.

In an embodiment Rl is Ci-₄ haloalkyl, R2 is Ci-₄ alkyl or Ci-₄ haloalkyl, R5 and R6 are independantly Ci_₄ alkyl optionally substituted with hydroxyl and n is 1.

In an embodiment Rl is Ci-₄ haloalkyl, R2 is Ci-₄ alkyl or Ci-₄ haloalkyl, R5 and R6 together with the ca rbon atom to which they are attached, form a 5- or 6-membered heterocycloalkyi, wherein said heterocycloalkyi is optionally substituted with Ci-₄ alkyl and n is 1.

In an embodiment Rl is Ci-₄ haloalkyl, R2 is Ci-₄ alkyl or Ci-₄ haloalkyl, R3 is Ci_₄ alkyl and R4 is oxo.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, Ci_₄ haloalkyl or halogen, R3 is Ci_₄ alkyl optionally substituted with hydroxyl and R4 is oxo.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R4 is oxo and R5 and R6 are hyd roxy-Ci_₄ alkyl. In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R4 is oxo and R5 and R6 are hydroxy-Ci_₄ alkyl.

In an embodiment Rl is Ci_₄ haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R4 is oxo and R5 and R6 are hydrogen .

In an embodiment Rl is Ci-₄ haloalkyl, R2 is Ci-₄ alkyl or Ci-₄ haloalkyl, R4 is oxo and R5 is hydrogen and R6 is Ci_₄ alkyl optiona lly substituted with hydroxyl. In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R4 is oxo and R5 and R6 are independantly Ci_₄ alkyl optionally substituted with hydroxyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R4 is oxo and R5 and R6 together with the ca rbon atom to which they are attached, form a 5- or 6- membered heterocycloalkyl, wherein said heterocycloa lkyl is optionally substituted with C_1-4 alkyl . In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo.

In an embodiment Rl is Ci_-4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a

pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof. An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a

pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a

pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof. An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a

pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a

pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_₄ alkyl or Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_-4 alkyl or Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optiona lly substituted with hydroxyl, R5 and R6 are hydrogen, n is 1 and R4 is oxo, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(i) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo, or a pha rmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(ii) wherein Rl is Ci_ 4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pha rmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof. An embodiment of the invention is a compound of general formula A(iii) wherein Rl is Ci-4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pha rmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(iv) wherein Rl is Ci-₄ haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is oxo, or a pha rmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_-4 haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci-₄ alkyl, n is 1 and R4 is hydrogen, or a pharmaceutically acceptable salt or solvate thereof.

An embodiment of the invention is a compound of general formula A(v) wherein Rl is Ci- 4 haloalkyl, R2 is Ci_₄ haloalkyl, R3 is Ci_₄ alkyl optionally substituted with hydroxyl, R5 and R6 are hydroxy-Ci_₄ alkyl, n is 1 and R4 is oxo, or a pha rmaceutically acceptable salt or solvate thereof.

The compounds of formula A may be obtained in crysta lline form either directly by concentration from an organic solvent or by crystallisation or recrystallisation from an organic solvent or mixture of said solvent and a cosolvent that may be organic or inorganic, such as water. The crystals may be isolated in essentially solvent-free form or as a solvate, such as a hydrate. The invention covers all crystalline modifications and forms and also mixtures thereof.

Compounds of formula A may comprise asymmetrically substituted (chiral) ca rbon atoms which give rise to the existence of isomeric forms, e.g . enantiomers a nd possibly diastereomers. The present invention relates to all such isomers, either in pure form or as mixtures thereof (e.g . racemates) . Pure stereoisomeric forms of the compounds and the intermediates of this invention may be obtained by the application of procedures known in the art. The various isomeric forms may be separated by physical separation methods such as selective crystallization and chromatographic techniques, e.g. liquid chromatography using chiral stationary phases. Enantiomers may be separated from each other by the selective crystallization of their diastereomeric salts with optically active acids. Alternatively, enantiomers may be separated by chromatographic techniques using chiral stationary phases. Said pure stereoisomeric forms may also be derived from the corresponding pure stereoisomeric forms of the appropriate starting materials, provided that the reaction occurs stereoselectively or stereospecifically.

Preferably, if a specific stereoisomer is desired, said compound will be synthesized by stereoselective or stereospecific methods of preparation. These methods will

advantageously employ chiral pure starting materials.

In a particular embodiment, the compound of the invention may be an isomer of general formula A(i)

A(i)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated above,

or a pharmaceutically acceptable salt or solvate thereof.

In an alternative embodiment, the compound may be an isomer of general formula A(ii)

A(ii)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated above,

or a pharmaceutically acceptable salt or solvate thereof.

In a particular embodiment, the compound of the invention may be an isomer of general formula A(iv)

A(iv)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated above,

or a pharmaceutically acceptable salt or solvate thereof.

In an alternative embodiment, the compound may be an isomer of general formula A(v)

A(v)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated above,

or a pharmaceutically acceptable salt or solvate thereof.

In an embodiment, a compound of the invention may be an isomer of general formula B(i)

B(i)

wherein RIO, Rll, R12, R13 are as indicated above, or a pharmaceutically acceptable salt thereof.

In an embodiment, a compound of the invention may be an isomer of general formula B(ii)

B(ii)

wherein RIO, Rll, R12, R13 are as indicated above, or a pharmaceutically acceptable salt thereof. An embodiment of the invention is the compound according to general formula B wherein RIO is hydrogen or -C(0)0(t-butyl);

Rll is selected from the group consisting of hydrogen and oxo;

R12 and R13 are independently selected from the group consisting of hydrogen, allyl and -C(0)Omethyl;

n is 1 or 2.

An embodiment of the invention is the compound according to general formula B selected from the group consisting of:

1- (2-methylphenyl)-octahydro-lH-pyrrolo[l,2-a][l,4]diazepin-7-one;

l-(2-methylphenyl)-octahydropyrrolo[l,2-a]piperazin-6-one benzyl N-(2-{2-[(2- methylphenyl)carbonyl]-5-oxopyrrolidin-l-yl}ethyl)carbamate ;

tert-butyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo [l,2-a]piperazine-2-carboxylate ;

2- tert-butyl 7-methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo [1,2-a] piperazine - 2,7 dicarboxylate;

(tert-butyl 1 -(2-methylphenyl)-6-oxohexahyd ropy rrolo[ 1,2-a] pyrazine-2( 1H)- carboxylate);

Methyl 7-methyl-l-(2-methylphenyl)-6-oxo-octahydropyrrolo{l,2-a} piperazine-7- carboxylate;

Methyl l-(2-methylphenyl)-6-oxo-octahyd ropy rrolo[ 1,2-a] pi perazine-7-carboxy late ; tert-butyl l-(2-methy I phenyl)-octahyd ropy rrolo[ 1,2-a] pi perazine-2-carboxy late;

l-(2-methy I phenyl)-octahyd ropy rrolo[ 1,2-a] piperazine; l-(2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazin-6-one hydrochloride salt;2-tert- butyl 7,7-dimethyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2,7,7- trica rboxylate;

7,7-dimethyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-7,7- dicarboxylate;

tert-butyl l-(2-methylphenyl)-6-oxo-7,7-bis(prop-2-en-l-yl)-octahydropyrrolo[ l,2- a]piperazine-2-ca rboxylate and

l-(2-methylphenyl)-7,7-bis(prop-2-en-l-yl)-octahydropyrrolo[ l,2-a]piperazin-6-one; or a pharmaceutically acceptable salt thereof.

Compounds of general formula B, B(i) and B(ii) may be used as intermediates in the preparation of compounds of general formula A, A(i) and A(ii).

Compounds of the invention, optionally in combination with other active compounds, may be useful for the prevention, treatment or amelioration of dermal diseases, e.g. pruritus, prurigo nodularis, chronic pruritus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, urticaria, psoriasis, Sezary syndrome, alopecia areata, scabies or vitiligo, or any other dermal disease or condition characterized by pruritus.

An embodiment of the invention is a compound according according to general formula A for use in the prevention, treatment or amelioration of prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, urticaria, mastocytosis and pruritus with chronic secondary scratch lesions.

An embodiment of the invention is a pharmaceutical composition comprising, as a therapeutically active ingredient, a compound according to general formula A and a pharmaceutically acceptable carrier or vehicle, together with one or more other therapeutically active compound(s).

An embodiment of the invention is a pharmaceutical composition comprising, as a therapeutically active ingredient, a compound according to general formula A and a pharmaceutically acceptable carrier or vehicle, optionally together with one or more other therapeutically active compound(s), suitable for topical administration. An embodiment the invention relates to a method of preventing, treating or a meliorating a condition involving pruritus of the skin, wherein the condition is selected from the group consisting of acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurological or psychosomatic/psychiatric origin, including endocrine a nd metabolic disorders, infections, haematological and

lymphoproliferative diseases, solid neoplasms and drug-induced pruritus; mastocytosis; pruritus of unknown cause; pruritus with chronic secondary scratch lesions, such as prurigo nodularis, and all types of prurigo; or a ny other dermal disease or condition characterized by pruritus, the method comprising applying, on the skin of a patient in need thereof, a therapeutically effective amount of a compound according to general formula A, optionally together with a pharmaceutically acceptable carrier or one or more excipients, optionally in combination with other therapeutically active compounds. An embodiment the invention relates to the use of a compound according to general formula A in the manufacture of a medicament for the prevention, treatment or amelioration of pruritic skin conditions , e.g . acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurologica l or psychosomatic/psychiatric origin, including endocrine and metabolic disorders, infections, haematological and lymphoproliferative diseases, solid neoplasms and drug-induced pruritus; mastocytosis; pruritus of unknown cause; pruritus with chronic secondary scratch lesions, such as prurigo nodula ris, and all types of prurigo; or any other dermal disease or condition characterized by pruritus. An embodiment of the invention relates to a pharmaceutica l composition comprising, as a therapeutically active ingredient, a compound according to general formula A and a pharmaceutically acceptable carrier or vehicle. An embodiment of the invention relates to a pharmaceutical composition suitable for topical administration comprising, comprising as a therapeutically active ingredient, a compound according to general formula A and a pharmaceutically acceptable carrier or vehicle.

An embodiment of the invention relates to a method of preventing, treating or ameliorating a condition involving pruritus of the skin, the method comprising applying, on the skin of a patient in need thereof, a therapeutically effective amount of a compound according to general formula A.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of prurigo.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of lichen planus.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of atopic dermatitis. In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of eczema .

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of contact dermatitis.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of allergic dermatitis.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of nummular dermatitis.

In an embodiment compounds of the invention may be useful in the prevention, treatment or amelioration of lichen simplex. In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of psoriasis. In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of Sezary syndrome.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of cutaneous lymphomas.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of urticaria. In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of mastocytosis.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of pruritus with chronic secondary scratch lesions.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of acute pruritus in any condition.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of chronic pruritus on diseased skin.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of pruritic diseases on non-diseased skin of systemic origin. In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of pruritic diseases on non-diseased skin of neurological or psychosomatic/psychiatric origin.

In an embodiment compounds of general formula A may be useful in the prevention, treatment or amelioration of pruritus of unknown cause.

Besides being useful for human treatment, the compounds of the present invention may also be useful for veterinary treatment of animals including mammals such as horses, cattle, sheep, pigs, dogs, and cats.

PHARMACEUTICAL COMPOSITIONS OF THE INVENTION For use in therapy, compounds of the present invention are typically in the form of a pharmaceutical composition. The invention therefore relates to a pharmaceutical composition comprising a compound of formula A, optionally together with one or more other therapeutically active compound(s), together with a pharmaceutically acceptable excipient or vehicle. The excipient must be "acceptable" in the sense of being compatible with the other ingredients of the composition and not deleterious to the recipient thereof.

Conveniently, the active ingredient comprises from 0.05-99.9% by weight of the formulation.

In the form of a dosage unit, the compound may be administered one or more times a day at appropriate intervals, always depending, however, on the condition of the patient, and in accordance with the prescription made by the medical practitioner. Conveniently, a dosage unit of a formulation contain between 0.1 mg and 1000 mg, preferably between 1 mg and 100 mg, such as 5-50 mg of a compound of formula A.

A suitable dosage of the compound of the invention will depend, inter alia, on the age and condition of the patient, the severity of the disease to be treated and other factors well known to the practising physician. The compound may be administered orally, parenterally or topically according to different dosing schedules, e.g. daily or with weekly intervals. In general a single dose will be in the range from 0.01 to 400 mg/kg body weight. The compound may be administered as a bolus (i.e. the entire daily dosis is administered at once) or in divided doses two or more times a day. In the context of topical treatment it may be more appropriate to refer to a "usage unit", which denotes a single dose which is capable of being administered to a patient, and which may be readily handled and packed, remaining as a physically and chemically stable unit dose comprising either the active material as such or a mixture of it with solid or liquid pharmaceutical diluents or carriers.

The term "usage unit" in connection with topical use means a unitary, i.e. a single dose capable of being administered topically to a patient in an application per square centimetre of the infected area of from 0.1 mg to 10 mg and preferably from 0.2 mg to 1 mg of the active ingredient in question. It is also envisaged that in certain treatment regimes, administration with longer intervals, e.g. every other day, every week, or even with longer intervals may be beneficial. If the treatment involves administration of another therapeutically active compound it is recommended to consult Goodman & Gilman's The Pharmacological Basis of

Therapeutics, 9^th Ed., J.G. Hardman and L.E. Limbird (Eds.), McGraw-Hill 1995, for useful dosages of said compounds. The administration of a compound of the present invention with one or more other active compounds may be either concomitantly or sequentially.

The formulations include e.g. those in a form suitable for oral (including sustained or timed release), rectal, parenteral (including subcutaneous, intraperitoneal,

intramuscular, intraarticular and intravenous), transdermal, ophthalmic, topical, dermal, nasal, buccal or intradermal administration. Topical administration of the claimed formulation is particularly suitable.

The formulations may conveniently be presented in dosage unit form and may be pre- pared by any of the methods well known in the art of pharmacy, e.g. as disclosed in Remington, The Science and Practice of Pharmacy, 20^th ed., 2000. All methods include the step of bringing the active ingredient into association with the carrier, which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing the active ingredient into association with a liquid carrier or a finely divided solid carrier or both, and then, if necessary, shaping the product into the desired formulation.

Formulations of the present invention suitable for oral administration may be in the form of discrete units as capsules, sachets, tablets or lozenges, each containing a prede- termined amount of the active ingredient; in the form of a powder or granules; in the form of a solution or a suspension in an aqueous liquid or non-aqueous liquid, such as ethanol or glycerol; or in the form of an oil-in-water emulsion or a water-in-oil emulsion. Such oils may be edible oils, such as e.g. cottonseed oil, sesame oil, coconut oil or peanut oil. Suitable dispersing or suspending agents for aqueous suspensions include synthetic or natural gums such as tragacanth, alginate, acacia, dextran, sodium carboxymethylcellulose, gelatin, methylcellulose, hydroxypropylmethylcellulose, hydroxypropylcellulose, carbomers and polyvinylpyrrolidone. The active ingredients may also be administered in the form of a bolus, electuary or paste.

A tablet may be made by compressing or moulding the active ingredient optionally with one or more accessory ingredients. Compressed tablets may be prepared by

compressing, in a suitable machine, the active ingredient(s) in a free-flowing form such as a powder or granules, optionally mixed by a binder, such as e.g. lactose, glucose, starch, gelatine, acacia gum, tragacanth gum, sodium alginate, carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, polyethylene glycol, waxes or the like; a lubricant such as e.g. sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride or the like; a disintegrating agent such as e.g. starch, methylcellulose, agar, bentonite, croscarmellose sodium, sodium starch glycollate, crospovidone or the like or a dispersing agent, such as polysorbate 80.

Moulded tablets may be made by moulding, in a suitable machine, a mixture of the powdered active ingredient and suitable carrier moistened with an inert liquid diluent.

Formulations for rectal administration may be in the form of suppositories in which the compound of the present invention is admixed with low melting water soluble or insoluble solids such as cocoa butter, hydrogenated vegetable oils, polyethylene glycol or fatty acids esters of polyethylene glycols, while elixirs may be prepared using myristyl palmitate.

Formulations suitable for parenteral administration conveniently comprise a sterile oily or aqueous preparation of the active ingredients, which is preferably isotonic with the blood of the recipient, e.g. isotonic saline, isotonic glucose solution or buffer solution. The formulation may be conveniently sterilised by for instance filtration through a bacteria retaining filter, addition of sterilising agent to the formulation, irradiation of the formulation or heating of the formulation. Liposomal formulations as disclosed in e.g. Encyclopedia of Pharmaceutical Technology, vol.9, 1994, are also suitable for parenteral administration.

Alternatively, the compounds of formula A may be presented as a sterile, solid preparation, e.g. a freeze-dried powder, which is readily dissolved in a sterile solvent immediately prior to use. Transdermal formulations may be in the form of a plaster, patch, microneedles, liposomal or nanoparticulate delivery systems or other cutaneous formulations applied to the skin. Formulations suitable for ophthalmic administration may be in the form of a sterile aqueous preparation of the active ingredients, which may be in microcrystalline form, for example, in the form of an aqueous microcrystalline suspension. Liposomal formulations or biodegradable polymer systems e.g. as disclosed in Encyclopedia of Pharmaceutical Technology, vol.2, 1989, may also be used to present the active ingredient for ophthal- mic administration.

Formulations suitable for topical, such as dermal, intradermal or ophthalmic administration include liquid or semi-liquid preparations such as liniments, lotions, gels, sprays, micro or nano-emulsions, oil-in-water or water-in-oil emulsions such as creams, ointments, pastes, applicants, foams, filmforming systems or microneedles; or solutions or suspensions such as drops. Compositions for ophthalmic treatment may preferably additionally contain a cyclodextrin.

For topical administration, the compound of formula A may typically be present in an amount of from 0.01 to 20% by weight of the composition, such as 0.1% to about 10 %, but may also be present in an amount of up to about 50% of the composition.

Formulations suitable for nasal or buccal administration include powder, self-propelling and spray formulations, such as aerosols and atomisers. Such formulations are disclosed in greater detail in e.g. Modern Pharmaceutics, 2^nd ed., G.S. Banker and C.T. Rhodes (Eds.), page 427-432, Marcel Dekker, New York; Modern Pharmaceutics, 3^th ed., G.S. Banker and C.T. Rhodes (Eds.), page 618-619 and 718-721, Marcel Dekker, New York and.Encyclopedia of Pharmaceutical Technology, vol. 10, J. Swarbrick and J.C. Boylan (Eds), page 191-221, Marcel Dekker, New York.

In addition to the aforementioned ingredients, the formulations of a compound of formula A may include one or more additional ingredients such as diluents, buffers, flavouring agents, colourant, surface active agents, thickeners, preservatives, e.g.

methyl hydroxybenzoate (including anti-oxidants), emulsifying agents and the like.

When the active ingredient is administered in the form of salts with pharmaceutically acceptable non-toxic acids, preferred salts are for instance easily water-soluble or slightly soluble in water, in order to obtain a particular and appropriate rate of absorption.

The pharmaceutical composition may additionally comprise one or more other active components conventionally used in the treatment of dermal disease or conditions, e.g . selected from the g roup consisting of glucocorticoids, vitamin D and vitamin D analogues, antihistamines, phosphodiesterase 4 (PDE4) inhibitors, JAK inhibitors, methylxanthines, β-adrenergic agents, COX-2 inhibitors, salicylates, indomethacin, flufenamate, naproxen, timegadine, retinoids, zinc salts, salicylazosulfapyridine a nd ca lcineurin inhibitors.

The term "compound of formula A" as used herein is intended to include compounds of formula A(i), formula A(ii), formula A(iii),formula A(iv) or formula A(v) .. The invention is further described in the appended examples which are not in any way intended to limit the scope of the invention as claimed.

METHODS OF PREPARATION The compounds of the present invention can be prepared in a number of ways well known to those skilled in the art of synthesis. The compounds of formula A may for example be prepared using the reactions and techniques outlined below together with methods known in the art of synthetic organic chemistry, or variations thereof as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. The reactions are carried out in solvents appropriate to the reagents and materials employed and suitable for the transformations being effected . Also, in the synthetic methods described below, it is to be understood that all proposed reaction conditions, including choice of solvent, reaction atmosphere, reaction temperature, duration of experiment and work-up procedures, a re chosen to be conditions of standard for that reaction, which should be readily recognized by one skilled in the art of orga nic synthesis. Not all compounds falling into a given class may be compatible with some of the reaction conditions required in some of the methods described . Such restrictions to the substituents which are compatible with the reaction conditions will be readily apparent to one skilled in the art and alternative methods can be used . Starting materials of general formula I are prepared according to standard procedures known to a chemist skilled in the art of organic synthesis. A benzyl halide derivative of formula I is treated with methylamine in a suitable solvent (e.g. methanol) under suitable conditions (e.g. RT to 50°C) for a suitable period of time (e.g. 3-5h) to form a compound of general formula II.

II

R1 , R2 = H, Me, CI, F, CF₃

Y= H, Me

X = CI, Br

Scheme 1

Starting material of formula IV is prepared according to standard procedures known to a chemist skilled in the art of organic synthesis. An acetophenone derivative of formula III can be converted into the chirally pure compound of formula IV according to a published procedure (PCT Int. Appl., 2008090117). Thus, reacting III with methylamine in a suitable solvent (e.g. methanol) under suitable conditions (e.g. RT to 50°C) for a suitable period of time (e.g. 3-5h), followed by addition of a suitable reducing agent (e.g. NaBH₄) and treatment, under suitable conditions, with a suitable chiral acid (e.g. L(+)-Malic acid) and subsequent basic treatment (e.g . with NaOH), compound IV is obtained.

Ill IV

Scheme 2

A compound of general formula VII can be prepared as described in Scheme 3. A diamine derivative of general formula V is treated with a suitable acylating agent (e.g. benzyl chloroformate) in a suitable solvent (e.g. DCM), under suitable conditions (e.g. 0°C to RT) for a suitable period of time (e.g. 3h) to form a compound of general formula VI, which in turn is treated with pentynoic acid in the presence of suitable coupling agents (e.g. EDCI, HOBT), in a suitable solvent (e.g. DCM), under suitable conditions (e.g. 0°C to RT) in the presence of a suitable base (e.g. TEA) for a suitable period of time (e.g. 12h) to form a compound of general formula VII.

Scheme 3

A compound of general formula VIII can be prepared as described in Scheme 4. A compound of general formula VII is treated with 2-Iodotoluene in a suitable solvent (e.g DMF), in the presence of a suitable base (e.g. TEA), under suitable coupling conditions (e.g. catalytic amounts of copper iodide and a palladium catalyst such as PdCI₂(PPh₃)₂), for a suitable period of time (e.g. 3h) at a suitable temperature (e.g . RT) to form a compound of general formula VIII.

Scheme 4

A compound of general formula IX can be prepared as described in Scheme 5. A compound of general formula VIII is treated with a suitable oxidizing agent (e.g. PIFA) in a suitable solvent (e.g. TFEA) for a suitable period of time (e.g. 3h) at a suitable temperature (e.g. 0°C to RT) to form a compound of general formula IX.

Scheme 5

A compound of general formula X can be prepared as described in Scheme 6. A compound of general formula IX is treated with a suitable acid agent (e.g. hydrobromic acid in acetic acid), in the presence of a suitable agent (e.g. titanium isopropoxide) and a suitable agent (e.g . PIFA) in a suitable solvent (e.g. TFEA) for a suitable period of time (e.g. 3h) at a suitable temperature (e.g. 0°C to RT) to form a compound of general formula IX. Alternatively, a compound of general formula IX can be treated under suitable hydrogenation conditions (e.g. 5 Atm H₂) in a suitable acidic media (e.g.

HCI/MeOH) for a suitable period of time (e.g . 24h) and in the presence of a suitable catalyst (e.g. Pd C 5%) to afford a compound of general formula X.

Scheme 6

A compound of general formula XI can be prepared as described in Scheme 7. A compound of general formula X is treated with a suitable acylating agent ( e.g.

triphosgene) in a suitable solvent (e.g . EtOAc) in the presence of a compound of general formula II or IV and of a suitable base (e.g. TEA), at a suitable temperature (e.g. 0°C to RT) for a suitable period of time (e.g. 3h) to afford a compound of general formula XI.

x XI

R1 , R2 = H, CH3. CI, F, CFs

Y= H, CHs

Scheme 7

A compound of general formula XIII can be prepared as described in Scheme 8. A compound of formula general X is treated with a suitable acylating agent (e.g. Boc anhydride) in the presence of a suitable base (e.g. TEA) in a suitable solvent (e.g. DCM) at a suitable temperature (e.g. RT) for a suitable period of time (e.g. 12h) to give a compound of formula XII, which in turn can be treated with a suitable acylating or alkylating agent (methyl chloroformate (possibly followed by Mel), allyl bromide) in the presence of a suitable base (e.g. LHMDS) in a suitable solvent (e.g. THF) at a suitable temperature (e.g. -78°C to 0°C) for a suitable period of time (e.g. 3h). The resulting compound (XIII, R₄=Boc) can in turn be treated with a suitable acid (e.g. TFA) in a suitable solvent (e.g. DCM) to afford a compound of general formula XIII (R = H).

Scheme 8

A compound of general formula XIV can be prepared as described in Scheme 9. A compound of general formula XII is treated as described for compound of general formula XI to give the urea derivative of general formula XIV. Further elaboration of V, V residues, using standard methods well described in the literature and well known to those skilled in the art (e.g. cleavage of an allylic double bond by ozonolysis to form the corresponding aldehyde and subsequent reduction of the aldehyde to form the corresponding alcohol, derivatization of the alcohol to form a mesylate) can lead to further derivatives also represented in the general formula XIV

Scheme 9

A compound of general formula XV can be prepared as described in Scheme 10. A compound of general formula XIV (where W=W'=CH₂CHO) is treated with methylamine under suitable reductive amination conditions (e.g . NABH₃(CN) in MeOH at RT for 12h) to give a compound of general formula XV.

Scheme 10

A compound of general formula XVI can be prepared as described in Scheme 11. A compound of general formula XIV (where W = H, W = CH₂OMs) is treated with a suita ble base (e.g . pyrrolidine) in a suitable solvent (e.g . THF) at a suitable temperature (e.g . 65°C) a nd for a suitable period of time (e.g . 20h) to give a compound of general formula XVI.

Scheme 11 A compound of general formula XVII can be prepared as described in Scheme 12. A compound of general formula XIV (where W = W = COOMe) is treated with a suitable salt (e.g. calcium chloride) and a suitable reducing agent (e.g. NaBH₄) in a suitable solvent (e.g. MeOH) at a suitable temperature (e.g. 0°C to RT) for a suitable period of time (e.g. 0.5h) to ive a compound of general formula XVII.

Scheme 12

A compound of general formula XVIII can be prepared as described in Scheme 13. A compound of general formula XIV (where W = H, W = CH₂OMs) is treated with a suitable amine (e.g. pyrrolidine, morpholine, N-methylpiperazine or N-acetylpiperazine) in a suitable solvent (e.g. THF) at a suitable temperature (e.g. 65°C) and for a suitable period of time (e.g. 20h) to give a compound of general formula XVIII.

Scheme 13

A compound of general formula XIX can be prepared as described in Scheme 14. A compound of general formula XIV is treated with a suitable alkylating agent (e.g. allyl chloride or bromide) in the presence of a suitable base (e.g. LHMDS) in a suitable solvent (e.g. THF) at a suitable temperature (e.g. -78°C to 0°C) for a suitable period of time (e.g. 3h) to give a compound of general formula XIX (where Y' = vinyl). Further elaboration of Y' residue, using standard methods well described in the literature and well known to those skilled in the art (e.g. cleavage of an allylic double bond by ozonolysis to form the corresponding aldehyde and subsequent reduction of the aldehyde to form the corresponding alcohol) can lead to further derivatives also represented in the general formula XIX.

A compound of general formula XX can be prepared as described in Scheme 15. A compound of general formula XIV is treated with a suitable reducing agent (e.g . borane dimethylsulfide) at a suitable temperature (e.g . RT) in a suitable solvent (e.g. MeOH) for a suitable period of time (e.g. 12h) to give a compound of general formula XX.

EXAMPLES

Some compounds are named using ACD/Name PRO 6.02 chemical naming software (Advanced Chemistry Development Inc., Toronto, Ontario, M5H2L3, Canada).

Proton Magnetic Resonance (NMR) spectra were recorded either on Varian instruments at 400, 500 MHz (Varian DirectDrive), or 600 MHz (INOVA 600 MHz), or on a Bruker instrument at 400 MHz spectrometers at 25°C. Chemical shifts are reported in ppm (δ) using the residual solvent line as internal standard. Peak multiplicities are expressed as follow: s, singlet; d, doublet; dd doublet of doublets, t, triplet; dt doublet of triplet; q, quartet; quin, quintet; m, multiplet; br s, broad singlet.

Total ion current (TIC) and DAD UV chromatographic traces together with MS and UV spectra associated with the peaks were taken also on a UPLC/PDA/MS Acquity™ system equipped with a Waters SQD mass spectrometer operating in positive and/or negative electrospray ionisation mode. [LC/MS/ES (+/-) : analyses performed using an Acquity™ UPLC BEH C18 column (50 x 21 mm, 1.7 μιη particle size), column temperature 40°C, mobile phase: A = 10 mM ammonium bicarbonate aqueous solution adjusted to pH 10 with ammonia and B = MeCN, Flow rate: 1.0 mL/min, Gradient: t=0 min 3% B, t= 1.50 min 99.9% B, t= 1.90 min 99.9% B, t=2.0 min 3% B.

Achiral purification were carried out using a mass directed autopurification system (MDAP) fractionlynx™ (Waters) operated under high pH chromatographic conditions mobile phase: A = 10 mM ammonium bicarbonate aqueous solution adjusted to pH 10 with ammonia and B = MeCN, flow rate 17 ml/min and column XBridge Prep. C18 5 μιη OBD (100mm x 19.0mm) @ room T.

Mass spectra (MS) were acquired on an Agilent HP1100 pump coupled with an Agilent MSD Trap XCT mass spectrometer operating in ES(+) and ES(-) ionization mode:

analysis performed using a Waters X-Bridge C18 column (50mm x 4.6 mm) at 40°C : A = 10 mM ammonium bicarbonate aqueous solution adjusted to pH 10 with ammonia and B = MeCN, Flow rate: 1.0 mL/min, Gradient: t=0 min 3% B, t=7.0 min 99% B, t= 8.0 min 99% B, 8.01 min 3% B, hold for 2 min, post run =3 min.

For the chiral separation and the chiral quality control two different techniques were used : 1) Supercritical Fluid Choromatography (SFC) : analytical chromatography was performed on a Berger SFC Analytix, while for the preparative SFC, a Jasco preparative SFC system was used 2) High Performance Liquid Chromatography (HPLC) : chiral Preparative HPLC was performed using a Waters 600 HPLC system and Agilent series 1100 instrument, while for analytical chromatography an Agilent series 1100 HPLC was used.

Abbreviations:

AcOH : Acetic acid

EtOAc: ethyl acetate

CH : cyclohexane

Cy: cyclohexane

DCM : dichloromethane

DIBAL-H : Diisobutylaluminium hydride

DMSO: dimethylsulfoxide DMAP: 4-Dimethylaminopyridine

DMF: N,N-dimethylformamide

DMPU : l,3-Dimethyl-3,4,5,6-tetrahydro-2(lH)-pyrimidinone

EDCI. HCI : N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride

EtOH : ethanol

HOBT.H₂0: hydroxybenzotriazol monohydrate

HPLC: High Pressure Liquid Chromatography

LHMDS : lithium bis(trimethylsilyl)amide

Me: Methyl

MeCN : acetonitrile

MeOH : methanol

MS : Mass Spectrometry

Ms: Mesyl

NMR: Nuclear Magnetic Resonance

Pd(dppf)CI₂: [ l,l'-Bis(di phenyl phosphino)ferrocene]dichloropalladium(II)

PE: Petroleum Ether

iPr: isopropyl

PIFA ((bis(trifluoroacetoxy)iodo)benzene

RT: room temperature

ee: enantiomeric eccess

Rt: retention time

TEA: triethylamine

TFA: trifluoroacetic acid

TFEA: 2,2,2-trifluoroethanol

THF: tetrahydrofuran

TLC: Thin Layer Chromatography

UPLC: Ultra Performance Liquid Chromatography

In the procedures that follow, after each starting material, reference to a Description or Compound by number is typically provided. This is provided merely for assistance to the skilled chemist. Often the terminology enantiomer 1, enantiomer 2, stereoisomer 1, stereoisomer 2, diastereoisomer 1, diastereoisomer 2, isomer 1, isomer 2 is applied : the numbers 1 and 2 refer to the first eluting compound and to the second eluting compound, respectively, in the analytical experiment (generally HPLC, with chiral or achiral column) specified in the experimental part.

Intermediate 1 r( lR)- l-r3,5-bis(trifluoromethyl)phenyl1ethvn(methyl)amine

To a solution of 3,5-bistrifluoromethylacetophenone (5.0 g, 19.5 mmol) in MeOH (20 mL), a solution of methylamine 8M in EtOH (6. 1 ml_, 48.8 mmol) was added dropwise in 15 min at 25°C under nitrogen atmosphere. The mixture was stirred 24h. NaBH₄ was then added portion wise (0.46 g, 19.92 mmol) at 0°C. A second amount of NaBH₄ was added over 30 min. (0.29 g) and the mixture stirred for a further 1.5h and the solvent evaporated under vacuo. EtOAc (40 mL) was added . L(+)-malic acid was then added portion wise ( 1.96 g, 14.6 mmol) . The suspension was stirred for 2h at 25°C, then 3h at 0°C. The suspension was filtered and the cake was washed with EtOAc and the solvent removed under vacuo to give a white solid (6.5 g) which was suspended in EtOAc (30 mL), then heated at reflux till complete dissolution and then cooled to 25°C. The suspension was filtered, washed with EtOAc then dried to give a solid (6.52 g) . The solid was stirred in a mixture of NaOH 10% ( 12 mL) and EtOAc ( 11 mL) . The organic layer was washed with water then concentrated to yield the title compound as a yellow oil

(4.78 g) . ^JH NMR (500 MHz, CDCI₃) δ ppm 7.81 (s, 2H), 7.77 (s, 1 H), 3.80 (q, .7=6.6 Hz, 1 H), 2.32 (s, 3H), 1.38 (d, .7=6.6 Hz, 3H) . HPLC: Column Chiralpa k IC (25 x 0.46 cm), 5μ. Mobile phase : n-Hexane/2-Propanol 99/1 v/v; Flow rate : l mL/min Detection : DAD t 220 nm, Rt=6.0 min .

Intermediate 2

methvK-f r3-(tnfluoromethyl)phenyl1 methyl )a mine

To a solution of methylamine 2M in MeOH (61.5 mL, 123.3 mmol), MeOH (30 mL) was added . The mixture was heated at 50°C under stirring and 3-(trifluoromethyl)benzyl chloride ( 1.6 mL, 10.3 mmol) dissolved in MeOH ( 10 mL) were added . The reaction mixture was stirred at this temperature for 5h . The solvent was removed under vacuo, then NaOH 1 M was added and the aqueous layer was extracted with DCM . The organic layer was filtered through a phase sepa rator and concentrated in vacuo to give 2.19 g of a colourless oil. *H NMR (400 MHz, CDCI₃) δ ppm 7.69 (s, 1H), 7.57 (d, 1H), 7.49 (t, 2H), 3.88 (s, 2H), 2.56, (s, 3H). UPLC-MS: Rt=0.39; m/z (ES+): 190 [M + H] ⁺ .

Intermediate 3

r(3,5-di methyl phenyl)methyl1(methyl)a mine

To a solution of methylamine 2M in MeOH (60.2 ml_, 120.5 mmol), MeOH (30 mL) was added. The mixture was heated at 50°C under stirring and 3,5-(dimethyl)benzyl bromide (2 g, 10.05 mmol) was added. The reaction mixture was stirred at this temperature for 5h. The solvent was removed under vacuo, then NaOH 1M was added and the aqueous layer was extracted with DCM. The organic layer was filtered through a phase separator and concentrated in vacuo to give 1.58 g of a crude that was purified on SP1 (SNAP-NH cartridge, 55g, CH/EtOAc 9:1 to 7:3 as eluent) to give the title compound as a colourless oil (1 g). H NMR (400 MHz, CDCI₃) δ ppm 7.33 (s, 1H), 7.07 (m, 2H), 6.92 (m, 1H), 3.79 (s, 2H), 2.57, (s, 3H). UPLC-MS: Rt=0.39; m/z (ES+): 150.0 [M + H] ⁺ .

Intermediate 4

- r3-fluoro-5-(trifluoromethyl)phenyl1 methyl XmethvDa mine

Methylamine 33% in MeOH (1.5 mL, 46.5 mmol) was dissolved in MeOH (15 mL). The mixture was heated at 50°C under stirring and l-(bromomethyl)-3-fluoro-5- (trifluoromethyl)benzene (1 g, 3.88 mmol) was added. The reaction mixture was stirred at this temperature for 3h. The solvent was removed under vacuo, then NaOH 1M (50 mL) was added and the aqueous layer was extracted with DCM (100 mL). The organic layer was dried over Na₂S0₄, filtered and evaporated under vacuo to give the title compound as a yellow oil (0.5 g). H NMR (400 MHz, CDCI₃) δ ppm 7.50 (s, 1H), 7.30 (m, 2H), 7.25 (m, 1H), 3.88 (s, 2H), 2.54, (s, 3H). UPLC-MS: Rt=0.51; m/z (ES+): 208.1 [M + H] ⁺ . Intermediate 5 Benzyl N-r2-(pent-4-vnamido) propyll carbamate

Pentynoic acid (0.267 g, 2.72 mmol) was added to a suspension of Z-propandiamine hydrochloride ( 1 g, 4 mmol), EDCI- HCI 767 mg, 4 mmol) a nd HOBt. H₂0 (540 mg, 4 mmol) in dry DCM (20 ml_) . The resulting mixture was cooled at 0°C a nd TEA ( 1.12 ml_, 8 mmol) was added dropwise. The reaction mixture was stirred at 25°C for 16h. The DCM solution was washed with NH₄CI solution (20 ml_ x 2) and NaHC0₃ solution, the organic phase was filtered through a phase separator and evaporated to dryness to obta in the title compound as a white solid (800 mg) . The crude product was used in the next step without further purification . ^JH NMR (400 MHz, CDCI₃) δ 7.41-7.31 (m, 5H), 6.20 (br s, 1 H), 5.27 (br s, 1 H), 5.12 (s, 2H), 3.34 (q , 2H), 3.27 (q , 2H), 2.59-2.52 (m, 2H), 2.42 (t, 2H), 2.02 (br s, 1 H) . UPLC-MS Rt=0.76; m/z (ES+) : 289 [M + H] ⁺ .

Intermediate 6

Benzyl N--T2-r5-(2-methylphenyl) pent-4-vnamidol propyl carbamate

Intermediate 5 (800 mg, 2.77 mmol) and 2-iodotoluene (335 μΙ_, 2.63 mmol) were charged in a two neck bottom flask equipped with vacuum/Argon system . They were dissolved in DMF (8 ml_), then TEA (425 μΙ_, 3.04 mmol), Cul (42 mg, 0.22 mmol) and PdCI₂(PPh₃)₂ (78 mg, 0.11 mmol) were added a nd the resulting mixture was stirred at 25 °C for 12h . DMF was removed in vacuo, the residue was dissolved in DCM and washed with HCI 1M, NaHC0₃ and brine. The layers were sepa rated and the organic one was filtered through a phase separator and evaporated to dryness to obtain a crude material which was purified on SPl (SNAP-Si0₂ ca rtridge, 50g, CH/EtOAc 4 : 6 to 0 : 1 as eluent) to give the title compound (726 mg) . ^JH NMR (400 MHz, CDCI₃) δ ppm 7.40-7.31 (m, 6H), 7.20-7.16 (m, 2H), 7.13-7.08 (m, 1 H), 6.26 (br s, 1 H), 5.26 (br s, 1 H), 5.10 (s, 2H), 3.35 (q, 2H), 3.23 (q, 2H), 2.81 (t, 2H), 2.51 (t, 2H), 2.40 (s, 3H), 1.66-1.61 (m, 2H). UPLC-MS: Rt=1.05; m/z (ES+): 379 [M + H] ⁺ .

Intermediate 7

Benzyl N-(2-- 2-r(2-methylphenyl^')carbonyl1-5-oxopyrrolidin-l-yl propyl^')carbamate

(racemate)

A solution of intermediate 6 (725 mg, 1.515 mmol) in TFEA (25 mL) was cooled and stirred at 0°C, then a solution of PIFA (1.235 g, 2.87 mmol) in TFEA (15 mL) was added dropwise. The reaction was left stirring at 0°C for 2h. Na₂C0₃1M solution was added to the reaction and the mixture was extracted several times with DCM. The phases were separated and the organic one was filtered through a phase separator and removed in vacuo. The crude material was purified on SP1 (SNAP-Si0₂ cartridge, 50 g, CH/EtOAc 5:5 to 0:1 as eluent) to give the title compound (677 mg). ^JH NMR (400 MHz, CDCI₃) δ ppm 7.66 (d, IH), 7.48 (t, IH), 7.40-7.30 (m, 7H), 5.65 (bt, IH), 5.15-5.07 (m, 3H), 3.75-3.65 (m, IH), 3.43-3.34 (m, IH), 3.19-3.09 (m, 2H), 2.53 (s, 3H), 2.51-2.31 (m, 3H), 2.02-1.93 (m, IH), 1.75-1.69 (m, 2H). UPLC-MS: Rt=0.99; m/z (ES+): 395

[M + H] ⁺ . Intermediate 8

l-(2-methylphenyl)-octahvdro-lH-pyrrolori,2-airi,41diazepin-7-one

(diastereomeric mixture)

Benzyl N-(2-l2-r(2-methylphenvncarbonyl1-5-oxopyrrolidin- l-yl propyl^')carbamate

(Intermediate 7, 211 mg) was dissolved in hydrobromic acid (33% in acetic acid) (2 mL) and the solution was stirred at room temperature for lh . The solvent was evaporated in vacuo and the residue was dissolved in ethanol (2 mL), titanium (IV) isopropoxide ( 1 mL) and TEA (23 mL) were added to the solution and the reaction mixture was stirred for 6h. NaBH₄ ( 10 mg) was added to the reaction mixture and the resulting solution was stirred l h at room temperature. An aqueous solution of ammonia was added, the precipitate was filtered off and the product was extracted with DCM . The crude was purified on N H-Silica ca rtridge (EtOAc as eluent) to give the title compound as a yellow oil (23 mg) . UPLC-MS : Rt=0.41 and 1.24; m/z (ES+) : 245.18 [M + H]^{+ J}H NMR (500 M Hz, CDCI₃)) δ ppm 7.53 (d, .7=7.6 Hz, 1 H), 7.26 (m, 3H), 4.04 (m, 2H), 3.76 (ddd, 3= 17 A, 11.2, 6.1 Hz, 1 H), 3.49 (br s, 1H), 3.29 (m, 1H), 2.65 (m, 1H), 2.37 (m, 4H), 2.01 (m, 2H) . Intermediate 9

Benzyl N-(2-aminoethyl) carbamate

A solution of benzylchloroformate ( 1.3 mL, 9 mmol) in DCM (25 mL) was added over 1.5h to a solution of 1,2-diaminoethane (6 mL, 90 mmol) in DCM (95 mL) cooled at 0°C. The solution was stirred for 2h at 0°C, then the solution was washed with brine (40 mL) . The organic phase was filtered through a phase separator and evaporated to dryness to obta in the title compound as a white solid ( 1.85 g) which was used in the next step without further purification. ^JH NMR (400 M Hz, CDCI₃) δ ppm 7.42-7.31 (m, 5H), 5.13 (br s, 3H), 3.27 (dd, 2H), 2.85 (t, 2H) . UPLC-MS : Rt=0.46; m/z (ES+) : 195 [M + H] ⁺ .

Intermediate 10

Benzyl N-r2-(pent-4-vnamido) ethyll carbamate

O

Pentynoic acid (0.590 g, 6 mmol) was added to a suspension of Intermediate 9 ( 1.8 g, 9 mmol), EDCI- HCI ( 1.72 g, 9 mmol) and HOBt. H₂0 ( 1.21 g, 9 mmol) in dry DCM (30 mL) . The resulting mixture was cooled to 0°C and TEA ( 1.25 mL, 9 mmol) was added dropwise. The reaction mixture was stirred at 25°C for 12h . The DCM solution was washed with NH₄CI solution ( 15 mL) and NaHC0₃ solution (15 mL), the organic phase was filtered through a phase sepa rator and evaporated to dryness to give the title compound as a white solid ( 1.97 g) . The crude product was used in the next step without further purification. ^JH NMR (400 M Hz, CDCI₃) δ ppm 7.40-7.34 (m, 5H), 6.15 (br s, IH), 5.17 (br s, I H), 5.12 (s, 2H), 3.46-3.34 (m, 4H), 2.52 (dt 2H), 2.38 (t, 2H), 2.0 (br s, I H) . UPLC-MS : Rt=0.75; m/z (ES+) : 275 [M + H] ⁺ .

Intermediate 11

Benzyl N--T2-[5-(2-methylphenyl) pent-4-ynamidol ethyl carbamate

Intermediate 10 (500 mg, 1.52 mmol) and 2-iodotoluene ( 186 μί, 1.45 mmol) were charged in a two necks round bottom flask equipped with vacuo/Argon system. They were solubilized in DMF (5 mL), then TEA (235 μί, 1.67 mmol), Cul (22 mg, 0.12 mmol) and PdCI₂(PPh₃)2 (41 mg, 0.06 mmol) were added and the resulting mixture was stirred at 25°C for 3h . DMF was removed in vacuo, the residue was dissolved in DCM and washed with NH₄CI solution ( 15 mL) and NaHC0₃ solution (15 mL) . The organic phase was filtered through a phase sepa rator and evaporated to dryness to obtain a yellow crude material which was purified on SP1 (SNAP-Si0₂ cartridge, 25g, CH/EtOAc 9.5 : 0.5 to 4 : 6 as eluent) to give the title compound as a white off solid (370 mg) . ¹ NMR (400 MHz, CDCI₃) δ ppm 7.40-7.31 (m, 6H), 7.20-7.17 (m, 2H), 7.13-7.09 (m, I H), 6.22 (br s, I H), 5.16 (m, I H), 5.09 (s, 2H), 3.48-3.40 (m, 2H), 3.40-3.33 (m, 2H), 2.79 (t, 2H), 2.49 (t, 2H), 2.41 (s, 3H) . UPLC-MS : Rt= 1.07; m/z (ES+) : 365 [M + H] ⁺ .

Intermediate 12

Benzyl N-(2-- 2-[(2-methylphenyl)carbonyll-5-oxopyrrolidin- l-yl ethyl)carbamate

(racemate)

A solution of intermediate 11 (370 mg, 1.016 mmol) in TFEA (13 mL) was cooled and stirred at 0°C, then a solution of PIFA (656 mg, 1.52 mmol) in TFEA (7 mL) was added dropwise. The reaction was left stirring at 0°C for 3h. Na₂C0₃1M solution was added to the reaction and the mixture was extracted several times with DCM. The phases were separated and the organic one was filtered through a phase separator and removed in vacuo. The crude material was purified on SP1 (SNAP-Si0₂ cartridge, 25 g, CH/EtOAc 7:3 to 3:7 as eluent) to give the title compound as a white foam (300 mg).¹ NMR (400 MHz, CDCI₃) δ ppm 7.67 (d, IH), 7.47 (t, IH), 7.38-7.29 (m, 7H), 5.28 (br s, IH), 5.20 (bd, IH), 5.10 (q, 2H), 3.85-3.78 (m, IH), 3.61-3.51 (m, IH), 3.28-3.14 (m, 2H), 2.52 (s, 3H), 2.45-2.35 (m, IH), 2.32-2.19 (m, 2H), 1.94-1.86 (m, IH). UPLC-MS: Rt=0.99; m/z (ES+): 381 [M + H] ⁺

Intermediate 13

l-(2-methylphenyl)-octahydropyrrolo[l,2-alpiperazin-6-one benzyl N-(2--T2-[(2- methylphenyl)carbonyll-5-oxopyrrolidin-l-yl ethyl)carbamate

(racemic mixture, ANTI configuration at Cl-C8a

HCI 1M (5 mL) and Pd/C 5% (100 mg) were added to a solution of Intermediate 12 (790 mg, 2.076 mmol) in MeOH (80 mL). The reaction was left stirring under H₂ (5 atm) for 12 h. Then further HCI 1M (lmL) and Pd/C 5% (100 mg) were added and the reaction was left stirring under H₂ (5 atm), after 6h Pd/C 5% (50 mg) was added and the reaction was left stirring under H₂ (5 atm) for 12h. The catalyst was removed by filtration through a celite pad and the solvent was removed in vacuo. NaHC0₃ saturated solution and DCM were added to the residue, the two layers were separated and the organic phase was filtered through a phase separator and removed in vacuo. The crude material was purified on SP1 (SNAP-NH cartridge, CH/EtOAc 5:5 to 3:7 as eluent) to give the title compound as a colourless oil (240 mg).¹ NMR (400 MHz, CDCI₃) δ ppm 7.48 (dd, IH), 7.27-7.19 (m, 3H), 4.12 (dd, IH), 3.74-3.66 (m, IH), 3.62 (d, IH), 3.15 (dd, IH), 2.98 (dt, IH), 2.85 (dt, IH), 2.43 (s, 3H), 2.40-2.34 (m, 2H), 1.95-1.85 (m, IH), 1.61-1.52 (m, IH). UPLC-MS: Rt=0.36; m/z (ES+): 231 [M + H] ⁺ .

Intermediate 14

tert-butyl l-(2-methylphenyl)-6-oxo-octahvdropyrrolo ri,2-a1piperazine-2-carboxylate

(racemic mixture, ANTI configuration at Cl-C8a)

Intermediate 13, (306 mg, 1.33 mmol), was dissolved in 15 mL of DCM. To this solution, TEA (445 mL, 6 mmol) and Boc₂0 (378 mg, 1.7 mmol) were added and the reaction mixture was stirred at room temperature overnight. Water was added to the reaction and the two layers were separated, the organic layer was again washed with water, filtered through a phase separator and evaporated. The crude was purified by flash chromatography (28 g SNAP NH cartridge, eluting from CH/EtOAc 9:1 to 6:4). The fractions were collected and the solvent removed to give 356 mg of title compound. UPLC-MS: m/z (ES+): 331.23 [M + H]⁺ Rt=0.98 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.23-7.17 (m, 4H), 4.78-4.81 (d, IH), 4.48-4.44 (m, IH), 4.08-4.04 (m, IH), 3.77-3.66 (m, 2H), 3.66-3.56 (m, IH), 2.50-2.35 (m, IH), 2.44 (s, 3H), 2.02-1.92 (m, IH), 2.02- 1.92 (m, IH), 1.83-1.74 (m, IH), 1.18 (s, 9H).

Intermediate 15

2-tert-butyl 7-methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo [1,2-al piperazine -

2,7 dicarboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 14 (355 mg, 1.074 mmol) was dissolved in THF (15 ml_) under N₂ and the solution was cooled to -78°C; LHMDS 1M in THF (2.68 ml_, 2.68 mmol) was added and the reaction was left stirring at this temperature for 10 min and at -30°C for 15 min, then methylchloroformate (91.5 μΙ_, 1.18 mmol) was added and the reaction was left stirring for 20 min at 25°C. HCI IN aq was added, followed by EtOAc. The layers were separated, the aqueous one extracted several times with EtOAc. The organic phase was dried over Na₂S0₄, filtered and concentrated. The crude material was purified on SP1 (SNAP-NH cartridge, 28 g, CH/EtOAc 9: 1 to 1 : 1 as eluent) to give the title compound as a white solid (295 mg). UPLC-MS, m/z (ES+) : 389.26 [M + H]⁺ Rt= 1.03. *H NMR (400 MHz, CDC ) δ ppm 7.26-7.15 (m), 4.95-4.93 (d), 4.77-4.74 (m), 4.49-4.43 (m), 4.25- 4.19 (m), 4.06-4.00 (m), 3.80 (s), 3.75 (s), 3.73-3.62 (m), 3.60-3.45 (m), 2,49 (s), 2,43 (s), 2.36-2.28 (m), 2.25-2.17 (m), 2.04-1.97 (m), 1.18 (s), 1.17 (s). Intermediate 16

terf-butyl 1 -(2-methy I phenyl)-6-oxohexahyd ropy rrolo[ l ,2-a1pyrazine-2(l/-/)-carboxy late

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 15 (237 mg, 0.610 mmol) was dissolved in THF (10 ml_). The solution was cooled down to -78°C and LHMDS was added, the reaction was left stirring 20 min at this temperature and 20 min at 0°C. Methyl iodide (57 μί) was added and the reaction was left at 25°C for lh. HCI 1M, followed by EtOAc were added. The phases were separated and the aqueous one was extracted with more EtOAc. The organics were combined, dried over Na₂S0₄, filtered and concentrated. The crude was purified by Flash Chromatography (SNAP column) eluting from CH/EtOAc 9 : 1 to EtOAc 100%. The fractions were collected and the solvent removed in vacuo obtaining 85 mg of the title compound as a white foam . UPLC-MS : m/z (ES+) : 403.32 [M + H] ⁺ ; Rt= 1.08 min ^JH NMR (400 MHz, CDCI₃) δ ppm 7.26-7.14 (m), 4.97-4.94 (m), 4.48-4.45 (m), 4.05-4.02 (m), 3.81 (s), 3.77-3.64 (m), 3.58-3.49 (m), 2,45 (s), 2.43-2.37 (m), 1.88- 1.82 (m), 1.42 (s), 1.18 (s), 1.17 (s) .

Intermediate 17

Methyl 7-methyl- l-(2-methylphenyl)-6-oxo-octahvdropyrrolo-f l ,2-a piperazine-7- ca rboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 16 (80 mg, 0. 206 mmol) was dissolved in DCM (8 mL) and TFA ( 1 mL) was added dropwise. The reaction was left stirring at 25°C for 2h, then the solvent was removed in vacuo and the residue was dissolved in MeOH a nd filtered through an SCX ca rtridge eluting with NH₃ in MeOH 2M solution . The solvent was removed in vacuo to give 56 mg of the title compound . UPLC-MS : m/z (ES+) : 303.22 [M + H] ⁺ ; Rt=0.51.

Intermediate 18

Methylamine (3 g, 40% aqueous solution) was dissolved in 30 mL of MeOH . The reaction mixture was heated at 50°C under stirring . 3,5-Bis(trifluoromethy)-benzyl chloride (2 g, 7.6 mmol) dissolved in 10 mL of MeOH, was added . The solution was left stirring at this temperature for 5h . The solution was concentrated ca refully to remove MeOH as much as possible, then an aqueous solution of NaOH 1 M was added and the aqueous layer was extracted with DCM . The two phases were sepa rated ; the organic phase was filtered through a phase separator and removed carefully in vacuo obtaining the title compound (0.8 g) as a yellow oil. UPLC-MS: m/z (ES+): 258.01 [M + H]⁺ Rt=0.60. *H NMR (400 MHz, CDCI₃) δ ppm 7.83 (s, 2H), 7.79 (s, IH), 3.91 (s, 2H), 3.30 (m, IH), 2.50 (s, 3H); UPLC-MS: Rt=1.30; m/z (ES+): 586 [M + H] ⁺ . Intermediate 19

Methyl 2-(-fr3,5-bis(trifluoromethyl) phenyl! methyl XmethvDcarba moyl)-7-methyl- 1-(2- methylphenyl)-6-oxo-octahvdropyrrololl,2-a piperazine-7-carboxylate

(diastereomeric mixture with ANTI confi uration at Cl-C8a)

Triphosgene (22.44 mg, 0.07 mmol) was dissolved in EtOAc (1 mL), this solution was cooled at 0°C and a solution of Intermediate 17 (52 mg, 0.172 mmol) and TEA (40 μί, 0.46 mmol) in EtOAC (2 mL) was added. The resulting mixture was left stirring at this temperature for 2h, then TEA (40 μί, 0.46 mmol) and Intermediate 18 (61.91 mg, 0.240 mmol) in EtOAC (2 mL) were added and the mixture was left stirring for 3h. NaOH 1M was added to the mixture, the phases were separated and the organic layer was washed with HCI 1M and brine, dried over Na₂S0₄ and concentrated in vacuo. The crude material was purified on SP1 (snap-NH cartridge, 11 g, CH/EtOAc 9:1 to 0:1 as eluent) to give the title compound as a white foam (70 mg).¹H NMR (500 MHz, CDCI₃) δ ppm 7.67 (s, IH), 7.29 (s, 2H), 7.19 (s, 2H), 7.10 (s, 2H), 4.62 (d, IH), 4.28 (d, 1 H), 4.17 (d, IH), 4.13 (dt, IH), 3.73 (s, 3H), 3.68 (m, IH), 3.30 (m, IH), 3.12 (m, IH), 2.96 (m, IH), 2.89 (s, 3H), 2.17 (m, IH), 1.69 (m, IH), 1.31 (s, 2 H). UPLC-MS: Rt=1.30; m/z (ES+): 586 [M + H] ⁺ .

Intermediate 20

methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-7-carboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

To a 0°C cooled solution of intermediate 15 (86 mg, 0.22 mmol) in DCM (8 mL) was added TFA (2 mL) . The reaction mixture was stirred at 25°C for 2h . The solvent was removed in vacuo to give a crude that was purified on SCX ca rtridge (solution of ammonia 2M in MeOH as eluent) to give the title compound (63 mg) . ¹ N MR (400 MHz, CDCI₃) δ ppm 7.51-7.46 (m), 7.26-7.18 (m), 4.14-4.08 (m), 3.93-3.87 (m) 3.83-3.80 (m), 3.76-3.69 (m), 3.60-3.57 (m), 3.46-3.41 (m), 3.16-3.02 (m), 2.91-2.79 (m), 2.48 (s), 2.44-2.41 (m), 2.29-2.22 (m), 2.17-2.09 (m), 2.03- 1.95 (m), 1.85- 1.72 9m) .

UPLC-MS : Rt=0.46; m/z (ES+) : 289.18 [M + H] ⁺ .

Intermediate 21

methyl 2-(- [3 ,5-bis(trifluoromethyl)phenyll methyl (methyl)carbamoyl)- l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l ,2-al piperazine-7-carboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

To a 0 °C cooled solution of triphosgene (30 mg, 0.087 mmol) in EtOAc ( 1 mL) under stirring were added intermediate 20 (63 mg, 0.22 mmol) dissolved in EtOAc (2 mL) and TEA (50 μί, 0.59 mmol) . The reaction mixture was stirred at this temperature for 2h, then TEA (50 μί) and Intermediate 18 (79 mg, 0.3 mmol) dissolved in EtOAc (2 mL) were added . The reaction was stirred at 25°C for 3h, then NaOH 1 M, HCI I N and brine were added . The organic layer was dried over sodium sulphate, filtered and concentrated in vacuo to give a crude that was purified on SP1 (snap-NH cartridge, l lg, CH/EtOAc 8 : 2 to EtOAc as eluent) to give the title compound (60 mg) . H NMR (400 MHz, CDCI₃) δ ppm 7.74 (br s), 7.37 (br s), 7.19-7.11 (m), 4.72-4.67 (m), 4.36-4.32 (m), 4.24-4.20 (m), 4.18-4.16 (m), 4.06-4.04 (d), 3.96-3.90 (m), 3.82 (s), 3.77-3.71 (m), 3.52-3.46 (m), 3.45-3.43 (m), 3.41-3.36 (m), 3.27-3.14 (m), 3.05-2.92 (m), 2.58 (s), 2.52 (s), 2.24-2.17 (m), 2.13-2.09 (m), 1.95-1.87 (m), UPLC-MS : Rt= 1.27; m/z (ES+) : 572.28 [M + H] ⁺ .

Intermediate 22

terf-butyl l-(2-methylphenyn-octahydropyrrolo[ l ,2-alpiperazine-2-carboxylate

(racemic mixture with ANTI configuration at Cl-C8a)

To a 0°C cooled solution of a compound prepared as described for intermediate 14 (67 mg, 0.2 mmol) in THF (5 mL), a solution of borane dimethylsulfide complex 2M in THF (0.404 mL, 0.8 mmol) was added dropwise. The reaction mixture was stirred overnight at 25°C, then a solution of borane dimethylsulfide complex 2M in THF (0.101 mL) was added and the mixture was stirred at 25 °C for 8h. A solution of borane dimethylsulfide complex 2M in THF (0.101 mL) was added and the mixture was stirred overnight at 25°C. MeOH (6 mL) was carefully added and the reaction mixture was stirred at 25°C for 2h. HCI 1M was added and the mixture was stirred overnight. Saturated solution of NaHC0₃ was added, followed by EtOAc. The organic layer was dried over sodium sulphate, filtered and concentrated in vacuo, to give the title compound (60 mg) which was used in the next step without further purifications. UPLC-MS : Rt=0.74; m/z (ES+) : 317.27 [M + H] ⁺ .

Intermediate 23

l-(2-methylphenyl)-octahvdropyrrolor i ,2-a1piperazine

(racemic mixture with ANTI configuration at Cl-C8a)

Intermediate 22 (60 mg, 0.19 mmol) was dissolved in a solution of HCI 1.25 M in MeOH (8 ml_) and the reaction mixture was stirred over weekend at 25°C. The mixture was concentrated in vacuo, then NaOH 1 M was slowly added, followed by addition of DCM . The aqueous layer was extracted several times with DCM . The combined organic layers were filtered through a phase separator and concentrated in vacuo to give 50 mg of the title compound. *H NMR (400 MHz, CDCI₃) δ ppm 7.46 (d, I H), 7.21-7.14 (m, 3H), 3.83 (d, IH), 3.19-3.06 (m, 4H), 2.41 (s, 3H), 2.37-2.31 (m, I H), 2.24 (q, I H), 2.16-2.10 (m, I H), 1.83- 1.34 (m, 5H) . UPLC-MS : Rt=0.34; m/z (ES+) : 217.15 [M + H] ⁺ .

Intermediate 24

l-(2-methylphenv0-octahvdropyrrolor i ,2-a1 piperazin-6-one hydrochloride salt

(racemic mixture with ANTI configuration at Cl-C8a)

To a stirred solution of Intermediate 13 ( 1.9 g, 8.26 mmol) in Et₂0 (25ml_), was added Et₂O. HCI (5.0 ml_) dropwise at room temperature for 5 min and later stirred at that temperature for 30 min. Solvent was evaporated under reduced pressure and the salt formed was washed with EtOAc and dried to obtain 1.9 g of the title compound . ¹ NMR (500 MHz, DMSO- 6) δ ppm 9.74 (m, 2H), 7.79 (m, I H), 7.33 (m, 3H), 4.32 (dd,

.7= 11.2, 9.5 Hz, I H), 4.05 (m, 2H), 3.18 (m, I H), 2.42 (s, 3H), 2.27 (dd, .7=8.8, 6.4 Hz, I H), 1.79 (dtd, .7= 13.4, 7.8, 7.8, 6.6 Hz, I H), 1.42 (dtd, .7= 13.0, 9.0, 9.0, 6.6 Hz, I H) .

Intermediate 25 N-ir3,5-bis(trifluoromethyl) phenyl^"! methyl^"i--7- (hvdroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(first eluting enantiomeric pair with ANTI configuration at Cl-C8a)

To a stirred solution of Intermediate 21 (950 mg, 1.66 mmol) in MeOH (40 mL) was added calcium chloride (276 mg, 2.49 mmol). The resulting suspension was cooled to 0°C and sodium borohydride (188 mg, 4.98 mmol) was added portionwise. The reaction mixture was stirred at 25°C for 2h, then water (20 mL) was added . MeOH was evaporated under vacuo and the aqueous layer was extracted with DCM (3x50 mL). The organic layer was separated, dried over sodium sulphate, filtered and evaporated to give 950 mg of a beige foam which was subjected to semipreparative HPLC. Two fractions were obtained : Intermediate 25 (100 mg, first eluting pair of enantiomers) and

Intermediate 26 (280 mg, second eluting pair of enantiomers, described below).

Intermediate 25 : semipreparative HPLC, Rt= 11' 08". Columns: XTerra PREP MS C18 OBD 10 μιη 30 x 150 mm, room temperature; Injection volume: 300 μΙ (multiple injections); m/z (ES+) : 543.00 [M + H] ⁺ .

Intermediate 26

Ν--Γ [3, 5-bis(trifluoromethyl) phenyl] methyl^"i--7- (hydroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[ l ,2-alpiperazine-2-carboxamide

(second eluting enantiomeric pair with ANTI configuration at Cl-C8a)

Intermediate 26 : semipreparative HPLC: Rt= 11' 66". Columns : XTerra PREP MS C18 OBD 10 μιη 30 x 150 mm, room temperature; Injection volume : 300 μΙ (multiple injections) ; Solvents: A = 10 mM ammonium bicarbonate acqueous solution adjusted to pH 10 with ammonia ; B = Acetonitrile. UV Conditions: UV detection range: 210 nm to 350 nm; Acquisition rate : 1.0 spectra/s; m/z (ES+) : 543.00 [M + H] ⁺ .

Intermediate 27

2-tert-butyl 7, 7-di methyl l-(2-methylphenyl)-6-oxo-octa hvdropyrrolor i ,2-a1 piperazine- 2,7,7-tricarboxylate

(racemic mixture with ANTI configuration at Cl-C8a)

Intermediate 14 (400 mg, 1.21 mmol) was dissolved in THF ( 15 mL) and the solution was cooled to -78°C; LHMDS 1 M in THF (2.66 mL, 2.66 mmol) was added and the reaction was left stirring at this temperature for 10' and at -50°C for 15 min, then methylchloroformate ( 103 μί, 1.33 mmol) was added and the reaction was left stirring for 45 min while temperature gradually increased to 0°C. HCI I N aq (2 mL) was added and the mixture was diluted with water ( 15 mL), then extracted three times with EtOAc. The combined organic phases were dried over Na₂S0₄, filtered and concentrated in vacuo. The crude material was purified on SP1 (SNAP ca rtridge, 50 g, CH/EtOAc 4 : 6 to 1 : 9 as eluent) to give the title compound as a pale yellow foam (430 mg) . UPLC-MS, m/z (ES+) : 447.00 [M + H]⁺ Rt= 1.06. *H NMR (400 MHz, CDCI₃) δ ppm 7.25-7.13 (m, 4H), 4.85-4.81 (d, 1 H), 4.48-4.43 (m, 1 H), 4.07-4.00 (m, 1 H), 3.86 (s, 3H), 3.78 (s, 3H), 2.59-2.48 (m, 2H), 2.45 (s, 3H), 3.72-3.60 (m, 3H), 1.16 (s, 9H) .

Intermediate 28

7, 7-di methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l ,2-al piperazine-7,7- dicarboxylate

(racemic mixture with ANTI configuration at Cl-C8a)

To a 0°C cooled solution of Intermediate 27 (380 mg, 0.85 mmol) in DCM (20 mL) was added TFA (3 mL) . The reaction mixture was stirred at 25°C for 2h. The solvent was removed under vacuo to give a crude that was purified on SCX cartridge (solution of ammonia 2M in MeOH as eluent) to give the title compound (256 mg) . ¹H NMR (400 MHz, CDCI₃) δ ppm 7.48-7.42 (m, I H), 7.25-7.18 (m, 3H), 4.14 (dd, I H), 3.84 (s, 3H), 3.79 (s, 3H), 3.72-3.65 (m, 2H), 3.16 (dd, I H), 3.06 (td, I H), 2.88 (td, I H), 2.55-2.48 (m, I H), 2.44 (s, 3H), 2.32-2.25 (m, I H) . UPLC-MS : Rt=0.53; m/z (ES+) : 347.23

[M + H] ⁺

Intermediate 29

7, 7-di methyl 2-({ r3,5-bis(trifluoromethyl)phenyl1 methyl XmethvDcarba moyl)- 1-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1 piperazine-7,7-dicarboxylate

(racemic mixture w

To a 0°C cooled solution of triphosgene (88 mg, 0.30 mmol) in EtOAc (3 mL) under stirring were added Intermediate 28 (256 mg, 0.74 mmol) and TEA ( 150 pL, 1.08 mmol) dissolved in EtOAc (4 mL) . The reaction mixture was stirred at 0°C for 2h, then

Intermediate 18 (266 mg, 1.04 mmol) dissolved in EtOAc (4 mL) and TEA ( 150 pL, 1.08 mmol) were added . The reaction was stirred at 25°C for 3 hrs, then washed with NaOH 0.5N ( 10 mL), HCI IN ( 10 mL) and brine ( 10 mL) . The organic layer was dried over Na₂S0₄, filtered and concentrated in vacuo to give 482 mg of the title compound which was used in the next step without further purifications. ¹H NMR (400 MHz, CDCI₃) δ ppm 7.75 (br s, I H), 7.36 (br s, 2H), 7.27-7.23 (m, IH), 7.21-7.12 (m, 3H), 4.69 (d, I H), 4.34 (d, 1H), 4.22 (d, 1H), 4.13 (d, 1H), 3.86 (s, 3H), 3.84-3.75 (m, 4H), 3.38 (d, 1H), 3.25 (td, 1H), 3.04-2.94 (m, 4H), 2.55-2.46 (m, 4H), 2.43-2.35 (m, 1H). UPLC-MS: Rt=1.28; m/z (ES+): 630.32 [M + H] ⁺ .

Alternative procedure for preparation of Intermediate 29

7, 7-di methyl 2-f-f r3,5-bis(trifluoromethyl) phenyl! methyl XmethvDcarba moyl)- l-(2- methylphenyl)-6-oxo-octahvdropyrrolori,2-a1piperazine-7,7-dicarboxylate

(enantiomeric pair with ANTI confi uration at Cl-C8a)

Compound 16 (50 mg, 0.097 mmol) was dissolved in THF (3 ml_) under Ar and the solution was cooled to -78°C; LHMDS 1M in THF (0.2 ml_, 0.194mmol) was added and the reaction was left stirring at this temperature for 15 min and at -30°C for 20 min, then DMPU (l,3-Dimethyl-3,4,5,6-tetrahydro-2(lA7)-pyrimidinone) (28 μΙ_, 0.232 mmol) and methylchloroformate (10 μΙ_, 0.116 mmol) were added and the reaction was left stirring for lh at -30°C. Then the solution was cooled to -78°C and further LHMDS 1M in THF (0.200 mL, 0.194 mmol) and methylchloroformate (20 μί, 0.232 mmol) were added. After lh the reaction was allowed to reach -10°C, further LHMDS 1M in THF (0.400 mL, 0.388 mmol) and methylchloroformate (100 μί, 1.16 mmol) were added. After 30 min HCI IN aq was added, followed by EtOAc. The layers were separated, the aqueous one extracted several times with EtOAc. The organic phase was filtered through a phase separator and concentrated. The crude material was purified by flash

chromatography (SNAP Si0₂, cartridge, 10 g, CH/EtOAc 2:8 to EtOAc 100% as eluent) to give the title compound as a light yellow oil (36 mg). H NMR (400 MHz, CDCI₃) δ ppm 7.76 (s, 1H), 7.38 (s, 2H), 7.28-7.12 (m, 4H), 4.70 (d, 1H), 4.35 (d, 1H), 4.27-4.20 (m, 1H), 4.14(d, 1H),3.88 (s, 3H), 3.86-3.75 (m, 4H), 3.43-3.37 (m, 1H), 3.30-3.31 (m, 1H), 3.07-2.95 (m, 4H), 2.57-3.48 (m, 4H), 2,44-2.35 (m, 1H),. UPLC-MS, Rt=1.26, m/z (ES+): 629.9 [M + H] ⁺ . Intermediate 30 /V--fr3,5-bis(trifluoromethyl) phenyl^"! methyl - 7-(hvdroxymethyl)-/V-methyl-l-(2- methyl phenyl) -6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(diastereoisomeic mixture with ANTI configuration at Cl-C8a)

To a stirred solution of Intermediate 29 (36 mg, 0.057 mmol) in MeOH (5 ml_) was added calcium chloride (20 mg, 0.17 mmol). The resulting suspension was cooled to 0°C and sodium borohydride (13 mg, 0.34 mmol) was added. The reaction mixture was stirred at 25°C for 30 min, then H₂0 was added and MeOH was removed in vacuo. The aqueous layer was extracted several times with EtOAc and the combined organic layers were filtered through a phase separator and concentrated in vacuo to give a crude which was purified by flash chromatography (SNAP NH cartridge, 10 g, CH/EtOAc 8:2 to EtOAc/MeOH 9:1 as eluent) to give the title compound as a white foam (30 mg). ¹ NMR (400 MHz, CDCI₃) δ ppm 7.77 (s, 1H), 7.39 (s, 2H), 7.22 (m, 4H), 4.69 (d, 1H), 4.36 (d, 1H), 4.26-4.07 (m, 2H), 3.96-3.85 (m, 1H), 3.82-3.66 (m, 2H), 3.46-3.34 (m, 1H), 3.19 (td, 1H), 3.06-2.91 (m, 4H), 2.73-2.60 (m, 1H), 2.55 (s, 3H), 2.02-1.93 (m, 1H), 1.55 (m, 1H). UPLC-MS: Rt=1.15; m/z (ES+): 544.28 [M + H] ⁺ .

Intermediate 31

Ν--Γ1- [3, 5-bis(trifluoromethyl) phenyl] but-3-en-l-yl -N-methyl-l-(2-methylphenyl)-6- oxo-7-(prop-2-en-l-yl)-octahvdropyrrolori,2-a1piperazine-2-ca rboxamide

(mixture of stereoisomers with ANTI confi uration at Cl-C8a)

To a solution of Intermediate 13 (270 mg, 0.526 mmol) in dry THF (10 ml_) stirred at - 78 °C under nitrogen was added a 1M solution of LHMDS in THF (1.051 ml_, 1.051 mmol), followed after 15 min by the addition of DMPU (317 μΙ_, 2.63 mmol) and allylbromide (91.05 μΙ_, 1.05 mmol) . After stirring for 30 min at -78 °C, the temperature was slowly raised to -30°C and the mixture was stirred at this temperature for 40 min. The reaction was cooled again to -78°C and 1 ml_ more of LHMDS 1M THF solution was added followed by 50 μΙ_ of allylbromide. The reaction was left stirring at this

temperature for 15 min and then raised to -30°C and stirred for 30 min more, then the reaction was quenched by adding NH₄CI sat. sol . and extracted with EtOAc several times. The organic layer was d ried over Na₂S0₄, the solid was filtered out and the solvent removed in vacuo. The crude was purified by FC (SNAP 25 g, eluting from Cy 9/ EtOAc 1 to Cy 6 / EtOAc 4) . The fractions were collected and the solvent removed in vacuo obta ining 182.7 mg of the title compound . UPLC-MS, m/z (ES+) : 594.06 [M + H] ⁺

Rt= 1.43. H NMR (400 MHz, CDCI₃) δ ppm 7.72 (br s, I H), 7.35 (br s, 2H), 7.21-7.07 (m, 4H), 5.79-5.65 (m, 2H), 5.62-5.56 (m, I H), 5.21 (d, I H), 5.15 (d, IH), 5.05-5.02 (m, I H), 5.00 (br s, IH), 4.21-4.16 (m, I H), 4.03 (d, IH), 3.67-3.60 (m, I H), 3.30-3.24 (m, I H), 3.16-3.08 (m, I H), 2.85-2.75 (m, 5H), 2.66-2.56 (m, 2H), 2.54-2.46 (m, 4H), 2.20-2.12 (m, I H), 1.84- 1.77 (m, I H), 1.65- 1.58 (m, I H) .

Intermediate 32

N-- i-[3 ,5-bis(trifluoromethyl^')phenyll-3-oxopropyl -N-methyl- l-(2-methylphenyl^')-6- oxo-7-(2-oxoethyl)-octahydropyrrolo[ l ,2-a1 piperazine-2-carboxamide

(mixture of stereoisomers with ANTI confi uration at Cl-C8a)

A slow stream of 0₃ in 0₂ was passed through a -78°C cooled solution of Intermediate 31 ( 180 mg, 0.3 mmol) in DCM (30 ml_) until a pale blue colour persisted . Excess of 0₃ was purged by N₂ bubbling, then a solution of PPh₃ ( 120 mg, 0.45 mmol) in DCM (3 ml_) was added . The solution was allowed to reach 25°C and it was stirred for 12h . The solvent was removed in vacuo and the crude material was purified by flash

chromatography (SNAP-Si0₂ cartridge, 25g, eluting from CH/EtOAc 8 : 2 to EtOAc 100%) . The fractions were collected and the solvent removed in vacuo to give the title compound as white solid ( 130 mg) . H NMR (400 MHz, CDCI₃) δϋ ρριη 9.84 (s), 9.78 (s), 9.73 (d), 7.77 (s), 7.35 (s), 7.22-7.08 (m), 6.04-5.98 (m), 4.23-4.05 (m), 3.76-3.69 (m), 3.24-3.08 (m), 3.03-2.93 (m), 2.90-2.79 (m), 2.65-2.58 (m), 2.56 (s), 2.50 (s), 2.05-1.96 (m), 1.57-1.48 (m).

Intermediate 33

r2-f r3,5-bis(trifluoromethyl) phenyllmethyl methvOcarbamovO-l- (2-methylphenyl) - 6-oxo-octahvdropyrrolor i,2-a1 pi perazin-7-yll methyl methansulfonate

(diastereoisomeic mixture with ANTI configuration at Cl-C8a)

To a -5 °C cooled solution of Intermediate 30 (30 mg, 0.055 mmol) in DCM (2 mL), TEA (15 μΙ_, 0.11 mmol) was added followed by mesyl chloride (5 μΙ_, 0.06 mmol). The mixture was stirred for 30 min, then the organic phase was washed with HCI 0.5 N (2 mL), filtered through a phase separator and evaporated in vacuo to obtain the title compound ad pale yellow foam (34 mg) which was used without further purification. UPLC-MS : Rt= 1.20; m/z (ES+) : 621.7 [M + H] ⁺ .

Intermediate 34

tert-butyl l-(2-methylphenyl)-6-oxo-7,7-bis(prop-2-en-l-yl)-octahydropyrrolo[ l ,2- alpiperazine-2-ca rboxylate

(racemic mixture, ANTI configuration at Cl-C8a)

To a solution of Intermediate 14, (lg, 3.027 mmol) in lOOmL of THF dry stirred at -78°C under N₂ atmosphere, a solution of LHMDS 1M in THF (6.054 mL) was added, followed after 15min by DMPU (1.823ml, 15.13mmol) and allylbromide (524 μί, 6.054 mmol). After stirring at -78°C for 30min the temperature was slowly raised to -30°C and the mixture was stirred at this temperature for 40 min more. The mixture was cooled again to -78°C and more LHMDS was added (6.054 ml_) and left reacting for 30 min; another equivalent of LHMDS . water and EtOAc were added to the reaction and the two layers were separated, the organic layer was again dried over Na₂S0₄, the solid was filtered out and the solvent removed in vacuo. The crude was purified by flash chromatography (50 g SNAP cartridge, eluting from Cy/EtOAc 9:1 to 6:4). The fractions were collected and the solvent removed to give 1.021g of title compound. UPLC-MS: m/z (ES+): 410.96 [M + H]⁺ Rt=1.27 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.24-7.12 (m, 4H), 5.83-5.61 (m, 2H), 5.24-5 (m, 4H), 4.65 (d, IH), 4.46-4.36 (m, IH), 3.97-3.87 (m, IH), 3.79- 3.51 (m, 3H), 2.52-2.43 (m, IH), 2.42 (s, 3H), 2.35-2.26 (m, IH), 2.23-2.07 (m, 2H), 1.82-1.69 (m, 2H), 1.16 (s, 9H).

Intermediate 35

l-(2-methylphenyl)-7,7-bis(prop-2-en-l-yl)-octahydropyrrolo[l,2-alpiperazin-6-one

(racemic mixture, ANTI configuration at Cl-C8a)

Intermediate 34 (1.02 g, 2.487 mmol) was dissolved in DCM (60 mL) and TFA (5 mL) was added. The reaction was left stirring at room temperature for 3h, then the solvent was removed in vacuo and the residue was taken up with DCM and NaOH 1M. The phases were separated and the aqueous one extracted with more DCM. The organics were filtered through a phase separator and concentrated under vacuum obtaining 780 mg of the title compound. UPLC-MS: m/z (ES+): 312.10 [M + H]⁺ Rt=0.66 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.46-7.40 (m, IH), 7.27-7.17 (m, 3H), 5.81-5.65 (m, 2H), 5.18-5.05 (m, 4H), 4.12 (dd, IH), 3.62-3.47 (m, 2H), 3.14 (dd, IH), 3.02-2.92 (m, IH), 2.02-1.92 (m, IH), 2.87-2.77 (m, IH), 2.48 (dd, IH), 2.42 (s, 3H), 2.33 (dd, IH), 2.20- 2.08 (m, 2H), 1.77-1.66 (m, 2H), 1.06-1.52 (m, IH).

Intermediate 36

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)-6-oxo-7,7- bis(prop-2-en-l-yl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

Triphosgene (372.6 mg, 1.256 mmol) was dissolved in 20 mL of EtOAc, a solution of Intermediate 35 (780 mg, 2.51 mmol) and TEA (1 mL) in 50 mL of EtOAc was added at 0°C. The mixture was left stirring for 1.5h, then intermediate 18 (968.24 mL, 3.765 mmol) in 50 mL of EtOAc and TEA (ImL) were added and the reaction was left stirring at room temperature for 3h. Water was added to the mixture, the phases were separated, the aqueous one was extracted several times with more EtOAc and the combined organics were washed with HCI 1M aqueous solution. The organic layer was dried over Na₂S0₄, the solid was filtered out and the solvent removed in vacuo obtaining 1.5 g of the titled compound. The product was used in the next step without further

purification. MS: m/z (ES+): 594.07 [M + H]⁺ Rt=1.44 min. *H NMR (400 MHz, CDCI₃) δ ppm 7.75 (s, 1H), 7.37 (s, 2H), 7.27-7.11 (m, 4H), 5.81-5.6 (m, 2H), 5.25-5.01 (m, 4H), 4.68 (d, 1H), 4.38 (d, 1H), 4.23-4.15 (m, 1H), 3.96 (d, 1H), 3.65-3.56 (m, 1H), 3.41-3.33 (m, 1H), 3.19-3.09 (m, 1H), 3.00-2.87( m, 4H), 2.59-2.46 (m, 4H), 2.36- 2.27 (m, 1H), 2.21-2.05 (m, 2H), 1.76-1.66 (m, 2H).

Intermediate 37

N-- [3,5-bis(trifluoromethyl)phenyllmethyl -N-methyl-l-(2-methylphenyl)-6-oxo-7,7- bis(2-oxoethyl)-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(racemic mixture, ANTI configuration at Cl-C8a)

A slow stream of 0₃ in 0₂ was passed through a -78°C cooled solution of intermediate 36 (1.5 g, 2.53 mmol) in DCM (300 mL) until a pale blue colour persisted. Excess of 0₃ was purged by N₂ bubbling, then a solution of PPh₃ (995 mg, 3.79 mmol) in DCM (10 mL) was added. The solution was allowed to reach 25°C and it was stirred for 12h. The solvent was removed in vacuo and the crude material was purified by flash

chromatography (SNAP-Si0₂ cartridge, 50 g, eluting from CH/EtOAc 8:2 to EtOAc 100%). The fractions were collected and the solvent removed in vacuo to give the title compound as white solid (620 mg). ^JH NMR (400 MHz, CDCI₃) δ Dppm 9.78 (s, IH), 9.67 (s, IH), 7.75 (s, IH), 7.38 (s, 2H), 7.22-7.08 (m, 3H), 4.70 (d, 2H), 4.41-4.30 (m, IH), 4.27-4.01 (m, 3H), 3.94-3.84 (m, IH), 3.47-3.37 (m, IH), 3.29-3.17 (m, IH), 3.15- 3.03 (m, IH), 2.98 (s, 3H), 2.91 (q, IH), 2.72 (q, IH), 2.57-2.47 (m, 4H), 1.96-1.85 (m, IH), 1.82-1.74 (m, IH).

Intermediate 38

N-- [3,5-bis(trifluoromethyl)phenyllmethyl -7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 30 (17 mg, 0.032 mmol) was dissolved in 2 mL of THF and cooled at 0°C. BH₃-Me₂S (63 μΐ) was added and the reaction was left stirring at 25°C for 8h, then HCI 1 M aq and MeOH were added and the reaction was left stirring over night, further MeOH was added and the reaction was left stirring 6h. The mixture was concentrated in vacuo and taken up with DCM and NaHC0₃ ss. The organic phase was filtered through a phase separator and removed in vacuo obtaining 15 mg of the title compound as

diastereoisomeic mixture. UPLC-MS: Rt=1.18 min and 1.24 min; m/z (ES+): 530.03

[M + H] ⁺ .

Intermediate 39

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-N-methyl-l-(2-methylphenyl)-6-oxo- 7,7-bis(prop-2-en-l-yl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Triphosgene (407 mg, 1.37 mmol) was dissolved in 40 mL of EtOAc, a solution of Intermediate 35 (850 mg, 2.74 mmol) and TEA ( 1.15 mL) in 85 mL of EtOAc was added at 0°C. The mixture was left stirring for 2h, then intermediate 1 ( 1.12vg, 4.11 mmol) in 40 mL of EtOAc and TEA ( 1.15 mL) were added and the reaction was left stirring at room temperature for 12h, then heated to 45°C for 48h. NaOH I N was added to the mixture, the phases were separated, the aqueous phase was extracted several times with EtOAc and the combined organics were washed with HCI 1M aqueous solution. The organic layer was dried over Na₂S0₄, the solid was filtered out and the solvent removed in vacuo obta ining 1.5 g of the title compound . The crude was purified by flash chromatog raphy (SNAP 50 g, eluting from CH/EtOAc 9 : 1 to CH/EtOAc 1 : 1). The fractions were collected and the solvent removed in vacuo to give the title compound ( 1.35 g) . UPLC-MS : m/z (ES+) : 608.04 [M + H]⁺ Rt= 1.45, 1.48 min. *H N MR (400 MHz, CDCI₃) δ ppm 7.80 (s), 7.74 (s), 7.56 (s), 7.36 (s), 7.29-7.11 (m), 5.83-5.53 (m), 5.27-5.01 (m), 4.24-4.16 (m), 4.08-3.97 (m), 3.82-3.54 (m), 3.36-3.23 (m), 3.20-3.07 (m), 2.83 (s), 2.71 (s), 2.59-2.45 (m), 2.37-2.27 (m), 2.22-2.06 (m), 1.77- 1.64 (m), 1.53 (d), 1.40 (d) .

Intermediate 40

N-r( lR)- l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-N-methyl- l-(2-methylphenyl)-6-oxo-

7,7-bis(2-oxoethyl)-octahvdropyrrolor i ,2-a1 piperazine-2-carboxamide

(diastereomeric mixture with ANTI configuration at Cl-C8a)

A slow stream of 0₃ in 0₂ was passed through a -78°C cooled solution of Intermediate 39 ( 1.35 g, 2.22 mmol) in DCM (200 mL) until a pale blue color persisted . Excess of 0₃ was purged by N₂ bubbling, then a solution of PPh₃ (875 mg, 3.33 mmol) in DCM (3 mL) was added. The solution was allowed to reach 25°C and then it was stirred for 12h. The solvent was removed in vacuo and the crude material was purified by flash

chromatography (SNAP-Si0₂ cartridge, 50 g, eluting from CH/EtOAc 9:1 to EtOAc 100%). The fractions were collected and the solvent removed in vacuo to give the title compound as a white solid (1.1 g). UPLC-MS: m/z (ES+): 611.99 [M + H]⁺ Rt=1.10, 1.14 min.

Intermediate 41 N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7,7-bis(2- hvdroxyethyl)-N-methyl-l-(2-methylphenyl)-6-oxo-octahvdropyrrolori,2-a1piperazine- carboxamide (diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 40 (1.1 g) was dissolved in MeOH (40 mL) and NaBH₄ (270 mg) was added at 0°C. The reaction was left stirring at this temperature for 30 min, then NH₄CI aq. Sat. sol. was added, the MeOH was removed in vacuo and the aqueous phase was extracted several times with DCM. The organic layer was filtered through a phase separator and concentrated in vacuo. The crude was purified by flash chromatography (25 g SNAP cartridge, eluting from DCM 100% to DCM/MeOH 95:5). The fractions were collected and the solvent removed to give 900 mg of title compound as a white foam. UPLC/MS: m/z (ES+): 616.03 [M + H]⁺ , Rt=1.08, 1.10 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.80 (s), 7.75 (s), 7.56 (s), 7.37 (s), 7.29-7.11 (m), 5.65-5.52 (m), 4.23-4.06 (m), 3.93-3.71 (m), 3.71-3.60 (m), 3.41-3.29 (m), 3.24-3.12 (m), 3.09-2.92 (m), 2.83 (s), 2.71 (s), 2.56 (s), 2.17 -1.68 (m), 1.54 (d), 1.43 (d). Intermediate 42

N-rriRVl-r3,5-bisrtnfluoromethvnphenyllethyll-7,7-bisr2-hvdroxyethvn-N-methyl-l-2- methylphenyl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(diastereomeric mixture with ANTI configuration at Cl-C8a)

To a 0°C cooled solution of Intermediate 41 (600 mg, 0.975 mmol) in THF (40 mL), a solution of borane dimethylsulfide complex 2M in THF (1.95 mL, 3.9 mmol) was added dropwise. The reaction mixture was stirred 24h at 25°C, then heated to 50°C for 8h, then stirred for further 12h at 25°C. MeOH (4 mL) was carefully added and the reaction mixture was stirred at 25°C for 48h. The solution was evaporated and the crude material was dissolved in DCM and washed with NaHC0₃. The organic phase was filtered through a phase separator. The solvent was removed in vacuo to give the title compound as a white foam (620 mg). UPLC/MS: m/z (ES+) : 602.14 [M+H]⁺, Rt=0.88, 0.90 min.

Intermediate 43

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl1ethyll-N-methyl-l-(2-methylphenyl)- octahydropyrrolo[ l,2-alpiperazine-2-carboxamide

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Triphosgene (142 mg, 0.48 mmol) was dissolved in 25 mL of EtOAc, a solution of Intermediate 23 (260 mg, 1.2 mmol) and TEA (0.6 mL) in 20 mL of EtOAc was added at 0°C. The mixture was left stirring for 2h, then Intermediate 1 (455 mg, 1.68 mmol) in 20 mL of EtOAc and TEA (0.6 mL) were added and the reaction was left stirring at room temperature for 3 days. Water was added to the mixture, the phases were separated, the aqueous phase was extracted several times with EtOAc and the combined organics dried over Na₂S0₄, the solid was filtered out and the solvent removed in vacuo. The crude was purified by Flash Chromatography (SNAP NH eluting from Cy/EtOAC 9/1 to 0/1) The fractions were collected and the solvent removed in vacuo obtaining 337mg of the titled compound. Column : Chiralcel OD-H (25 x 0.46 cm), 5 um; Mobile phase: n- Hexane/2-Propanol 95/5 % v/v; Diast. 1 : 50 % a/a by UV (3.9 min); Diast. 2 : 50 % a/a by UV (5.3 min). Intermediate 44

Methyl -r rf lRI- l-rS.S-bisftrifluoromethvnphenyllethylKmethvncarbamoyl - l- (2-methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-7-ca rboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Triphosgene (330.8 mg, 1.11 mmol) was dissolved in 30 ml_ of EtOAc, a solution of Intermediate 20 (804 mg, 2.787 mmol) and TEA (1.2 mL) in 40 mL of EtOAc was added at 0°C. The mixture was left stirring for 2h, then Intermediate 1 (1.058 gr, 3.9 mmol) in 30 mL of EtOAc and TEA (1.2 mL) were added and the reaction was left stirring at room temperature for 3 days. Then 1 eq more of Intermediate 1 in 3 mL of EtOAc was added and the reaction was left stirring at RT 4 days more and heated at 40°C for 5h. The mixture was cooled and water was added, the layers were separated. The organic one was washed twice with HCI lm aq.sol. The phases were separated and the organics were dried over Na₂S0₄. The solid was filtered out and the solvent removed in vacuo. The crude was purified by Flash Chromatography (50g SNAP Cy/EtOAc from 9/1 to 0/1). The fractions were collected and concentrated in vacuo obtaining 1.075g of the title compound. UPLC/MS : m/z (ES+) : 586.06 [M + H]⁺ Rt= 1.26 min (isomer 1) and RT= 1.28 (isomer 2). ^JH NMR (400 MHz, CDCI₃) δ ppm 7.80 (s), 7.73 (s), 7.56.(s), 7.36 (s), 7.28- 7.18 (m), 5.66-5.52 (m), 4.27-4.11 (m), 4.08-4.01 (m), 4.01-3.87 (m), 3.84-3.81 (m), 3.8-3.76 (m), 3.74 (s), 3.54-3.39 (m), 3.38-3.12 (m), 3.09-2.88(m), 2.83 (s), 2.73- 2.70 (m), 2.6 (bs), 2.56-2.52 (m), 2.27-2.16 (m), 2.16-2.08 (m), 1.99-1.85 (m), 1.55- 1.49 (d), 1.45-1.38 (m).

Intermediate 45

methyl 2-- r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1(methyl)carbamoyl -l-

(2-methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-7-ca rboxylate

(mixture 1, ANTI configuration at Cl-C8a)

1.075g of Intermediate 44 were purified by chiral preparative HPLC obtaining two fractions. After evaporation were obtained : 400mg of Intermediate 45 (mixture 1, described here) and 395 of Intermediate 46 (mixture 2, described in the next

experimental part). Intermediate 45 : UPLC/MS: m/z (ES+) : 586.06 [M + H]⁺ Rt= 1.26 min. ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.80 (s), 7.56 (s), 7.28-7.11 (m), 5.61- 5.51 (m), 4.71-4.52 (m), 4.28-4.14 (m), 4.09-3.9 (m), 3.83 (s), 3.80-3.71 (m), 3.55- 3.38 (m), 3.34-3.11 (m), 3.10-2.93 (m), 2.71 (bs), 2.60 (s), 2.54 (s), 2.26-2.18 (m), 2.15-2.07 (m), 1.96-1.85 (m), 1.67 (bs), 1.45-1.39 (m).

Intermediate 46

methyl 2-- r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1(methyl)carbamoyl -l-

(2-methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-7-ca rboxylate

(mixture 2, ANTI configuration at Cl-C8a)

UPLC/MS : m/z (ES+) : 586.06 [M + H]⁺ Rt= 1.28 min. ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (s), 7.37 (s), 7.28-7.10 (m), 5.66-5.56 (m), 4.27-4.14 (m), 4.08-4.01 (m), 3.96-3.86 (m), 3.83 (s), 3.74 (s), 3.73-3.66 (m), 3.54-3.39 (m), 3.40-3.30 (m), 3.29- 3.10 (m), 3.06-2.89 (m), 2.83 (s), 2.60 (s), 2.54 (s), 2.26-2.06 (m), 1.99-1.89 (m), 1.56-1.50 (d).

Intermediate 47

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7-(hvdroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(diasterisomeric mixture 1, ANTI configuration at Cl-C8a)

Intermediate 45 (400 mg) was dissolved in MeOH (20 mL). To this solution, CaCI₂ (113.2 mg, 1.02 mmol) was added, the suspension was cooled to 0°C and NaBH₄ (77.52 mg) was added. The reaction was left stirring at room temperature for 2h. Then the mixture was concentrated under vacuum and the residue taken up with DCM and HCI 1M. The layers were separated and the organic layer was filtered through a phase separator and concentrated in vacuo obtaining 300 mg of the title compound. UPLC/MS : m/z (ES+) : 558.02 [M + H]⁺ Rt= 1.14 min and 1.15 min. CHLOROFORM-d) δ ppm 7.80 (s), 7.56 (s), 7.28-7.11 (m), 5.61-5.51 (m), 4.25-4.04 (m), 3.96-3.65 (m), 3.36-3.11 (m), 3.07-2.95 (m), 2.72 (s), 2.55 (s), 2.02-1.91 (s), 1.88-1.68 (m), 1.57-1.39 (m).

Intermediate 48

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl1ethyll-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(diasterisomeric mixture 2, ANTI configuration at Cl-C8a)

Intermediate 47 (395 mg) was dissolved in MeOH (20 mL). To the solution CaCI₂

(112.2mg, l .Ol lmmol) was added, the suspension was cooled down to 0°C and NaBH₄ (76.55 mg,) was added. The reaction was left stirring at room temperature for 2h. Then the mixture was concentrated under vacuum and the residue taken up with DCM and HCI 1M. The layers were separated and the organic was filtered through a phase separator and concentrated in vacuo obtaining 350 mg of the title compound. UPLC/MS: m/z (ES+) : 558.02 [M + H]⁺ Rt= 1.15 min and 1.17 min. ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (s), 7.37 (s), 7.32-7.08 (m), 5.66-5.51 (m), 4.28-4.00 (m), 3.99-3.81 (m), 3.80-3.61 (m), 3.43-3.25 (m), 3.25-3.10 (m), 3.07-2.87 (m), 2.84 (s), 2.81-2.59 (m), 2.55 (s), 2.01-1.91 (m), 1.89-1.80 (m), 1.78-1.66 (m), 1.56-1.49 (m). Intermediate 49

N-- r3,5-bis(trifluoromethyl^')phenyl1methyl -7,7-bis(2-hvdroxyethyl^')-N-methyl-l-(2- methylphenvn-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(diasterisomeric mixture 2, ANTI configuration at Cl-C8a)

NaBH₄ (28 mg, 0.74 mmol), was added to an ice-cooled solution of Intermediate 37 (110 mg, 0.84 mmol) in MeOH (8 mL). The reaction mixture was stirred at 0°C for 40 min then NH₄CI aq. Sat. sol. (5 mL) was added, MeOH was evaporated and the aqueous solution was extracted several times with DCM. DCM was filtered through a phase separator and evaporated to give a crude that was purified on SP1 - Si0₂ lOg cartridge, DCM to DCM/MeOH 85 : 15 as eluent) to give the title compound as a white solid (20 mg). UPLC-MS, Rt= 1.05, m/z (ES+) : 602.1 [M + H] ⁺ . Intermediate 50 (2-- [(lR)-l-[3,5-bis(trifluoromethyl)phenyllethyl1(methyl)carbamoyl - l-(2-methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-alpiperazin-7-yl) methyl

methanesulfonate

(diasterisomeric mixture, ANTI configuration at Cl-C8a)

To a -5°C cooled solution of Intermediate 47 (2.07 g, 3.71 mmol) and TEA (1.034 mL, 7.42 mmol) in dry DCM (45 mL) a solution of mesyl chloride (0.32 mL, 4.08 mmol) in dry DCM (5 mL) was added dropwise. The reaction mixture was stirred at -5°C for 30 min, then washed with HCI 0.5 N aq . Sol. (3x35 mL). The organic layer was dried on Na₂S0₄, filtered and concentrated to give the title compound as a pale yellow foam (2.3 g). UPLC-MS, Rt= 1.23 and 1.25, m/z (ES+) : 636.0 [M + H] ⁺ .

Intermediate 51

(lS,8aS)-l-o-tolylhexahvdropyrrolor i,2-a1pyrazin-6(7/-/)-one

Intermediate 51 was obtained (white solid, 16.6 g) by SFC separation of Intermediate 24. Rt= 5.89 min (Chiral HPLC, Chiralpak AS-H column (15 x 0.46 cm), 3μ, mobile phase: Ethanol/Diethylamine 100/0.1 v/v, Flow rate: 0.6 mL/min. Detection : DAD at 220 nm).

Intermediate 52

(lS,8aS)-tert-butyl 6-oxo-l-o-tolylhexahvdropyrrolor i ,2-a1pyrazine-2(l/-/)-carboxylate

To a solution of Intermediate 51 (6 g, 26 mmol) in DCM (50 mL) was added TEA (5.3 g, 52 mmol), DMAP (317 mg, 2.6 mmol) and Boc₂0 (8.6 g, 39 mmol). The reaction mixture was stirred at 40 °C overnight and quenched with water. The resulting mixture was washed with water (2x 50 mL) and the combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (7 g, yield : 81%); m/z (ES+) : 331 [M + H] ⁺ .

Intermediate 53

(lS,8aS)-tert-butyl 7,7-diallyl-6-oxo-l-o-tolylhexahvdropyrrolor i,2-a1pyrazine-2(l/-/)- ca rboxylate

To a solution of Intermediate 52 (2.2 g, 6.7 mmol) in anhydrous THF (100 mL) under N₂ atmosphere, was added LiHMDS (1 M in THF, 21 mL) at -78 °C. The reaction was stirred for 15 min, followed by addition of DMPU (2.7 g, 21 mmol) and allylbromide (1.8 g, 15 mmol). The reaction mixture was stirred at -78 °C for 30 min and allowed to warm to - 30 °C, and then stirred at this temperature for another 2 h. After quenched with water at -78 °C and the mixture was then extracted with EtOAc (2 x 50 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=2/l to 1/1) to give the title compound (2.3 g, yield : 84%); m/z (ES+) : 411 [M + H] ⁺ .

Intermediate 54

(lS,8aS)-7,7-diallyl-l-o-tolylhexahydropyrrolo[ l ,2-alpyrazin-6(7/-/)-one

To a solution of Intermediate 53 (2.3 g, 5.6 mmol) in DCM (60 mL) was added TFA (5 mL). The reaction was stirred at room temperature for 3 h and then neutralized with 1 M aqueous NaOH solution to pH = 8. The resulting mixture was extracted with DCM (2 x 30 mL). The organic layers were dried over anhydrous Na₂S0₄, and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (1.4 g, yield : 83%); m/z (ES+) : 311 [M + H] ⁺ .

Intermediate 55

l-(3-fluoro-5-(trifluoromethyl)phenyl)-/V-methylmethanamine

To a solution of l-(bromomethyl)-3-fluoro-5-(trifluoromethyl)benzene (257 mg, lmmol) in MeOH (5 mL) was added methanamine in MeOH (5 mL). The reaction was stirred at 50 °C for 16 h and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (200 mg, yield : 90%); m/z (ES+) : 222 [M + H] ⁺ . Intermediate 56

ilS,8aS)-7,7-diallyl-/V-i3-fluoro-5-itrifluoromethvnbenzvn-/V-methyl-6-oxo-l-o-

To a solution of triphosgene (24 mg, 0.08 mmol) in EtOAc (2 ml_) at 0 °C was added solution of Intermediate 54 (50 mg, 0.16 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 ml_). The mixture was stirred for 1.5 h, followed by addition of l-(3,5-bis(trifluoromethyl) phenyl)-N-methylmethanamine (50 mg, 0.24 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous

Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (20 mg, yield : 23%); m/z (ES+) : 544 [M + H] ⁺ .

Intermediate 57

(lS,8aS)-7,7-diallyl-/V-methyl-/V-(3-methyl-5-(trifluoromethyl)benzyl)-6-oxo-l-o-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA 49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of N-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)methanamine (97 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (130 mg, yield : 74.3%) as yellow solid; m/z (ES+) : 540 [M + H] ⁺ .

Intermediate 58

(lS,8aS)-7,7-diallyl-/V-(3-methoxy-5-(trifluoromethyl)benzyl)-/V-methyl-6-oxo-l-o-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 ml_) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 ml_). The mixture was stirred for 1.5 h, followed by addition of l-(3-methoxy-5-(trifluoromethyl)phenyl)-N-methylmethanamine (105 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (130 mg, yield : 73%) as yellow solid; m/z (ES+) : 556 [M + H] ⁺ .

Intermediate 59

(lS,8aS)-7,7-diallyl-/V-(3-chloro-5-(trifluoromethyl)benzyl)-/V-methyl-6-oxo-l-o-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of l-(3-chloro-5-(trifluoromethyl)phenyl)-N-methylmethanamine (107 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (123 mg, yield : 68%) as yellow solid; m/z (ES+) : 560 [M + H] ⁺ .

Intermediate 60

f lS.8aSV7.7-diallyl-yv-methyl-6-oxo-l-o-tolyl-yy-f3-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of N-methyl-l-(3-(trifluoromethyl)phenyl)methanamine (91 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (100 mg, yield : 59%) as yellow solid; m/z (ES+) : 526 [M + H] ⁺ . Intermediate 61

1 -(3, 5-bis(trifluoromethyl) phenyl) but-3-en-l-ol

To a solution of 3,5-bis(trifluoromethyl)benzaldehyde (10 g, 41 mmol) in THF (100 mL) was drop wise added allylmagnesium bromide (50 mL, 1 M in THF, 50 mmol) at -40 °C. The reaction mixture was stirred at room temperature for 5 h and then poured into saturated aqueous NH₄CI solution and extracted with EtOAc (2 x 100 ml_). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (800 mg, yield : 7%).

Intermediate 62

1 -(3, 5-bis(trifluoromethyl) phenyl) but-3-enyl methanesulfonate

To a solution of Intermediate 61 (0.8 g, 2.8 mmol) and TEA (0.75 g, 7.4 mmol) in DCM (10 ml_) was added MsCI (0.32 g, 2.8 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 3 h and poured into water and then extracted with EtOAc. The organic layer was dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EA= 10/1 to 3/1) to give the title compound (691 mg, yield : 68%).

Intermediate 63

-(3,5-bis(trifluoromethyl)phenyl)-/V-methylbut-3-en-l-amine

To a solution of Intermediate 62 (691 mg, 1.9 mmol) in THF (10 ml_) was added MeNH₂ (3 ml_, 1 M in THF, 3 mmol) at 0 °C. The reaction mixture was stirred at room

temperature for 16 h and poured into water, and then extracted with EtOAc. The organic layer was dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH= 10/l) to give the title compound (575 mg, yield : 100%); m/z (ES+) : 298 [M + H] ⁺ .

Intermediate 64 & 65

riS,8aS^')-7,7-diallyl-/V-ri-r3,5-bisrtrifluoromethvnphenvnbut-3-envn-/V-methyl-6-oxo-l- o-tolylhexahydropyrrolo[ l,2-alpyrazine-2(l/-/)-carboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of Intermediate 63 (144 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give Intermediate 64 (30 mg, yield : 15%) and Intermediate 65 (30 mg, yield : 15%) as yellow solid; m/z (ES+) : 634

[M + H] ⁺ .

Intermediate 66

riS,8aS^')-7,7-diallyl-/V-ri-r3,5-bisrtrifluoromethvnphenvnbut-3-envn-/V-methyl-6-oxo-l- o-tolylhexahvdropyrrolor i,2-a1pyrazine-2(l/-/)-carboxamide

A solution of l-(3,5-bis(trifluoromethyl)phenyl)propan-l-one (2 g, 7.4 mmol) in

MeNH₂/MeOH (10 mL) under N₂ atmosphere was stirred for 16 h. The resulting mixture was concentrated in high vacuum. The residue was dissolved in EtOAc (20 mL), washed with brine (10 mL). The organic layer was dried over anhydrous Na₂S0₄ and

concentrated . The residue was disolved in THF (15 mL) followed by addition of NaBH₄ (400 mg, 10.6 mmol) at 0 °C. The reaction mixture was allowed to warm to room temperature and stirred for 2 h. EtOAc (20 mL) was added and the organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give Intermediate 66 (750 mg, yield : 49%) as yellow solid; m/z (ES+) : 286 [M + H] ⁺ .

Intermediate 67 & 68 (lS,8aSV7,7-diallyl-/V-(l-(3,5-bis(tnfluoromethvnphenvnpropylV/V-methyl-6-oxo-l-o-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of Intermediate 66 (144 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (49 mg, 0.48 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give Intermediate 67 (50 mg, yield : 25%) and Intermediate 68 (50 mg, yield : 25%) as yellow solid; m/z (ES+) : 622

[M + H] ⁺ .

Intermediate 69

To a solution of 3-bromo-5-(trifluoromethyl)benzoic acid (50 g, 186 mmol) in DCM (500 mL) at 0 °C, was added Oxalyl chloride (30.7 g, 242 mmol) with catalytical amount of DMF (0.5 mL). After stirring for 30 min the reaction mixture was concentrated. To a suspension of Ν,Ο-dimethylhydroxylamine hydrochloride (23.5 g, 242 mmol) in DCM (300 mL) at 0 °C was added TEA (51 g, 500 mol). Then a solution of acid chloride in DCM (300 mL) was added slowly. After stirring for 1 h, the reaction mixture was poured into water (200 mL) with vigorous stirring, extracted with DCM (2 x 200 mL). The organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄ and then concentrated . The residue was purified by silica gel chromatography (PE/EtOAc=20/l to 5/1) to give the title compound (47 g, yield : 81%); m/z (ES+) : 312 [M + H] ⁺ .

Intermediate 70 -bromo-5-(trifluoromethyl)benzaldehvde

To a solution of Intermediate 69 (47 g, 150 mmol) in THF (400 mL), was added DIBAL-H (120 mL, 1.5 M in toluene, 180 mmol) at -40 °C. The reaction was allowed to warm to room temperature slowly and stirred for 20 min. The reaction mixture was poured into water (200 mL) with vigorous stirring. The precipitate was filtered off and the filtrate was extracted with EtOAc (2 x 300 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄ and then concentrated. The crude was used directly without further purification.

Intermediate 71

-/V-(3-bromo-5-(trifluoromethyl)benzylidene)-2-methylpropane-2-sulfinamide

To a solution of Intermediate 70 (43 g, 169 mmol) in THF (400 mL) was added (S)-2- methylpropane-2-sulfinamide (22 g, 180 mmol) and Ti(0-iPr)₄ (62 g, 220 mmol) at 0 °C. After stirring for 6 h at room temperature, the reaction mixture was poured into a suspension of kieselguhr in water (200 mL) with vigorous stirring. The precipitate was filtered off and the filtrate was extracted with EtOAc (2 x 300 mL). The combined organic layers were washed with brine (50 mL), dried by anhydrous MgS0₄ and then

concentrated . The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (40 g, yield : 66%); m/z (ES+) : 356 [M + H] ⁺ .

Intermediate 72 & 63

(S)-/V-((R)-l-(3-bromo-5-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide, (S)-/V-((S)-l-(3-bromo-5-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

To a solution of Intermediate 70 (8 g, 22.5 mmol) in DCM (100 mL), was dropwise added methyl magnesium bromide (45 mL, 1M in THF, 45 mmol) at - 40 °C. After stirring for 2 h at room temperature, the reaction mixture was poured into saturated aqueous NH₄CI solution and extracted with DCM (2 x 100 mL). The combined organic layers were washed with brine (2 x 100 mL), dried by anhydrous MgS0₄ and then concentrated . The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the Intermediate 72 (R_f=0.30, PE/EtOAc=2/l) with (R)-Me (6.1 g, yield : 73%) and the Intermediate 73 (R_f=0.35, PE/EtOAc=2/l) with (S)-Me (1.2 g, yield : 14%). m/z (ES+); 372 [M + H] ⁺ .

Intermediate 74

(S)-/V-((R)-l-(3-bromo-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2- sulfinamide

To a solution of Intermediate 72 (6.1 g, 16.4 mmol) in THF (60 mL) under N₂ atmosphere was added LHMDS (32 mL, 1 M in THF, 32 mmol) at -60 °C. The reaction was stirred for 15 min followed by addition of Mel (4.5 g, 32 mmol). The reaction mixture was then stirred at room temperature for another 1 h and quenched with water at 0 °C. The resulting mixture was then extracted with EtOAc (2 x 100 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (5.1 g, yield : 80%); m/z (ES+) : 386 [M + H] ⁺ .

Intermediate 75

(S)-/V,2-dimethyl-/V-((R)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)propane-2- sulfinamide

A mixture of Intermediate 74 (1 g, 2.6 mmol), trimethylboroxine (328 mg, 2.6 mmol), Pd(PPh₃)₄ (300 mg, 0.26 mmol) and Cs₂C0₃ (1.7 g, 5.2 mmol) in DMF (12 mL) under N₂ atmosphere was microwaved at 110°C for 75 min. The reaction was poured into water (15 mL) and then extracted with EtOAc (2 x 30 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (591 mg, yield : 71%); m/z (ES+) : 322 [M + H] ⁺ .

Intermediate 76

-/V-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)ethanamine

A solution of Intermediate 74 (500 mg, 1.6 mmol) in HCI/MeOH (10 mL) was stirred for 15 min under N₂ atmosphere. The reaction was neutralized with 1 M NaOH to pH = 10-11 and then extracted with EtOAc (2 x 20 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated to give the title compound (300 mg, yield : 86%). m/z (ES+) : 218 [M + H] ⁺ .

Intermediate 77

riS,8aS^')-7,7-diallyl-/V-methyl-/V-rrR^')-l-r3-methyl-5-rtrifluoromethvnphenvnethvn-6-

To a solution of triphosgene (129 mg, 0.4 mmol) in EtOAc (5 mL) at 0 °C was added a solution of Intermediate 54 (300 mg, 1 mmol), DMAP (11 mg, 0.01 mmol) and TEA (293 mg, 2.9 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-N-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)ethanamine (273 mg, 1.26 mmol) in EtOAc (10 mL) and TEA (293 mg, 2.9 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc (2 X 30 mL). The combined organic layers were washed with 1 M aqueous HCI solution and then dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH=20/l to 10/1) to give the title compound (209 mg, yield : 39%) as yellow solid; m/z (ES+) : 554 [M + H] ⁺ .

Intermediate 78 (S)-/V-((S)-l-(3-bromo-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dim

sulfinamide

To a solution of Intermediate 73 (1.2 g, 3.2 mmol) in THF (60 mL) under N₂ atmosphere was added LHMDS (6.4 mL, 1 M in THF, 6.4 mmol) at -60 °C. The reaction was stirred for 15 min and followed by addition of Mel (0.69 g, 4.8 mmol) then stirred at room temperature for another 1 h. The reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 100 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (1.1 g, yield : 89%); m/z (ES+) : 386 [M + H] ⁺ .

Intermediate 79

(S)-/V,2-dimethyl-/V-((s)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)propane-2- sulfinamide

A mixture of Intermediate 78 (500 mg, 1.29 mmol), trimethyboroxine (328 mg, 2.6 mmol), Pd(PPh₃)₄ (142 mg, 0.129 mmol) and Cs₂C0₃ (844 mg, 2.59 mmol) in DMF (12 mL) under N₂ atmosphere was microwaved at 110 °C for 75 min. The reaction was poured into water (15 mL) and then extracted with EtOAc (2 x 30 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (380 mg, yield : 91%); m/z (ES+) : 322 [M + H] ⁺ . Intermediate 80

(R)-/V-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)ethanamine

A solution of Intermediate 79 (380 mg, 1.18 mmol) in HCI/MeOH (10 mL) was stirred for 15 min under N₂ atmosphere. The reaction was neutralized with 1 M NaOH solution (15 mL) to pH= 10-11 and then extracted with EtOAc (2 x 20 mL). The combined organic layers were dried by anhydrous Na₂S0₄ and concentrated to give the title compound (180 mg, yield : 70.3%); m/z (ES+) : 218 [M + H] ⁺ .

Intermediate 81

riS,8aS^')-7,7-diallyl-/V-methyl-/V-rrS^')-l-r3-methyl-5-rtrifluoromethvnphenvnethvn-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added a solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-N-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)ethanamine (105 mg, 0.48 mmol) and TEA (97 mg, 0.963 mmol) in EtOAc (2 mL). The reaction was stirred for 48 h at 50 °C and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (100 mg, yield : 56.3%) as yellow solid; m/z (ES+) : 554 [M + H] ⁺ .

Intermediate 82

To a mixture of 3,5-bis(trifluoromethyl)benzaldehyde (5 g, 20.7 mmol) and (S)-2- methylpropane-2-sulfinamide (3 g, 24.8 mmol) in DCM (50 ml) at 0 °C, was drop wise added Ti(0-iPr)₄ (5.9 g, 24.8 mmol) under N₂ atmosphere. After stirring for 20 h at room temperature, the reaction mixture was poured into water (100 mL) with vigorous stirring. The precipitate was filtered and the filtrate was extracted with DCM (2 x 150 mL). The combined organic layers were washed with brine (80 mL), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (6 g, yield : 84%); m/z (ES+) : 346 [M + H] ⁺ .

Intermediate 83 & 84

(S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)allyl)-2-methylpropane-2-sulfinamide (S)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)allyl)-2-methylpropane-2-sulfinamide

To a solution of Intermediate 82 (6 g, 17.4mmol) in DCM (100 mL) was drop wise added vinylmagnesium bromide (21 mL, 1 M in THF, 21 mmol) at -60 °C. The reaction mixture was stirred for 5 h at room temperature and poured into saturated aqueous NH₄CI solution. The resulting mixture was extracted with DCM (2 x 100 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄, and then concentrated . The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the (R)-Allyl-Intermediate 83 (2.6 g, yield : 40%) and (S)-Allyl-Intermediate 84 (1.4 g, yield : 21%); m/z (ES+) : 374 [M + H] ⁺ .

Intermediate 85

s(trifluoromethyl)phenyl)allyl)-/V,2-dimethylpropane-2-sulfinamide

To a solution of Intermediate 83 (2.6 g, 7 mmol) in THF (60 mL) under N₂ atmosphere was dropwise added LiHMDS (10.5 mL, 1 M in THF, 10.5 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (1.5 g, 10.5 mmol). The reaction was then stirred for another 3 h at room temperature and quenched with water at 0 °C. The resulting mixture was extracted with EtOAc (2 x 100 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (900 mg, yield : 30%); m/z (ES+) : 388 [M + H] ⁺ .

Intermediate 86

-l-(3,5-bis(trifluoromethyl)phenyl)-/V-methylprop-2-en-l-amine

A solution of Intermediate 85 (900 mg, 2.3 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution (15 mL) to pH= 10-11 and then extracted with EtOAc (2 x 20 mL). The organic layer was dried over anhydrous Na₂S0₄ and concentrated to give the title compound (500 mg, yield : 76%); m/z (ES+) : 284 [M + H] ⁺ .

Intermediate 87

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3,5-bisrtrifluoromethvnphenvnallvn-/V-methyl-6-oxo-l-o-

To a solution of triphosgene (95 mg, 0.33 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (200 mg, 0.65 mmol), DMAP (8 mg, 0.065 mmol) and TEA (200 mg, 1.95 mmol) in EtOAc (5 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3,5-bis(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (220 mg, 0.78 mmol) in EtOAc (5 mL) and TEA (200 mg, 1.95 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (100 mg, yield : 25%) as yellow solid; m/z (ES+) : 620 [M + H] ⁺ .

Intermediate 88

(S)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)allyl)-/V,2-dimethylpropane-2-sulfinamide

To a solution of Intermediate 84 (1.4 g, 3.8 mmol) in THF (20 mL) under N₂ atmosphere was dropwise added LiHMDS (4.5 mL, 1 M in THF, 4.5 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (0.5 g, 7.5 mmol). The mixture was stirred at room temperature for another 3 h and quenched with water at 0 °C. The resulting mixture was extracted with EtOAc (2 x 100 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography(PE/EtOAc=5/l to 2/1) to give the title compound (726 mg, yield : 50%); m/z (ES+) : 388 [M + H] ⁺ .

Intermediate 89

-l-(3,5-bis(trifluoromethyl)phenyl)-/V-methylprop-2-en-l-amine

A solution of Intermediate 88 (726 mg, 1.9 mmol) in HCI/MeOH (10 mL) was stirred for 15 min under N₂ atmosphere. The reaction was neutralized with 1 M NaOH solution (15 mL) to pH= 10-11 and then extracted with EtOAc (2 x 20 mL). The combined organic phase was washed with brine (10 mL), dried by Na₂S0₄, and then concentrated to give the title compound (400 mg, yield : 74%); m/z (ES+) : 284 [M + H] ⁺ . Intermediate 90

riS,8aS^')-7,7-diallyl-/V-rrS^')-l-r3,5-bisrtrifluoromethvnphenvnallvn-/V-methyl-6-oxo-l-o-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 ml_). The mixture was stirred for 1.5 h, followed by addition of (S)-l-(3,5-bis(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (136 mg, 0.48 mmol) in EtOAc (2 ml_) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (70 mg, yield : 34%) as yellow solid; m/z (ES+) : 620 [M+H] ⁺ .

Intermediate 81

f lS.8aSV7.7-diallyl-yv-methyl-6-oxo-l-o-tolyl-yv-ffRVl-f3-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 ml_) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 ml_). The mixture was stirred for 1.5 h, followed by addition of Methyl-[ l-(3-trifluoromethyl-phenyl)-ethyl]-amine (100 mg, 0.49 mmol) in EtOAc (2 ml.) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (82 mg, yield : 41%) as yellow solid; m/z (ES+) : 540 [M + H] ⁺ .

Intermediate 92

(S)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2- sulfinamide

To a solution of (S)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-2-methyl- propane-2-sulfinamide (1.5 g, 4.6 mmol) in anhydrous THF (20 mL) under N₂

atmosphere was dropwise added LHMDS (9.2 mL, 1 M in THF, 9.2 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C, followed by addition of Mel (1.04 g, 6.9 mmol). The reaction was stirred at room temperature for another 3 h and quenched with water at 0 °C. The resulting mixture was extracted with EtOAc (2 x 100 ml_). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography

(PE/EtOAc=5/l to 2/1) to give the title compound (1.2 g, yield : 76.5%); m/z (ES+) : 342 [M + H] ⁺ .

Intermediate 93

-l-(3-chloro-5-(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 92 (1.2 g, 3.5 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution (15 mL) to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic phase was washed with brine (10 mL), dried by Na₂S0₄, and then concentrated to give the title compound (750 mg, yield : 90%); m/z (ES+) : 238 [M + H] ⁺ .

Intermediate 94

riS,8aS^')-7,7-diallyl-/V-rrS^')-l-r3-chloro-5-rtrifluoromethvnphenvnethvn-/V-methyl-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (S)-l-(3-chloro-5-(trifluoromethyl)phenyl)-N-methylethanamine (114 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (50 mg, yield : 27%) as yellow solid; m/z (ES+) : 574 [M+H] ⁺ . Intermediate 95

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-chloro-5-rtrifluoromethvnphenvnethvn-/V-methyl-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-chloro-5-(trifluoromethyl)phenyl)-N-methylethanamine (100 mg, 0.42 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (65 mg, yield : 35%) as yellow solid; m/z (ES+) : 574 [M+H] ⁺ .

Intermediate 96

rSVA/,2-dimethyl-A/-rrR^')-l-r3-r4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-vn-5-

To a solution of Intermediate 74 (2.1 g, 5.4 mmol), Bis(pinacolato)diboron (1.5 g, 6 mmol), K₂C0₃ (1.38 g, 10 mmol) in 30 mL of THF/H₂0 (5 : 1) under N₂ atmosphere was added Pd(dppf)CI₂ (0.4 g, 0.5 mmol). The reaction was stirred for 5 h at 80 °C and quenched with water. The resulting was extracted with EtOAc (2 x 100 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (2 g, yield : 85%); m/z (ES+) : 434 [M+H] ⁺ .

Intermediate 97 (S)-/V-((R)- l-(3-hvdroxy-5-(trifluoromethyl)phenyl)ethyl)-/V,2-di methyl propa ne-2- sulfina mide

To a solution of Intermediate 96 (500 mg, 1.2 mmol) and NaOH ( 144 mg, 3.6 mmol) in THF ( 10 ml_), was added H₂0₂ ( 122 mg, 3.6 mmol) at 0 °C. The reaction mixture was allowed to wa rm to room tempraure and stirred for 2 h . The reaction was quenched with water and the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated to give the title compound (500 mg, yield : 134%) ; m/z (ES+) : 324 [M + H] ⁺ .

Intermediate 98

(S)-/V-((R)- l-(3-methoxy-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2- sulfina mide

To a solution of Intermediate 97 (500 mg, 1.54 mmol) in anhydrous THF ( 10 ml_) under N₂ atmosphere was added K₂C0₃ (414 mg, 2.98 mmol) and Mel (317 mg, 2.23 mmol) . The reaction mixture was stirred for 2 h and quenched with water. The resulting mixture was extracted with EtOAc (2 x 20 ml_) . The combined organic layers were washed with brine, dried over anhydrous Na₂S0₄ and then concentrated to give the title compound (500 mg, yield : 96%) ; m/z (ES+) : 338 [M + H] ⁺ .

Intermediate 99

(R)- l-(3-methoxy-5-(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 98 (500 mg, 1.48 mmol) in HCI/MeOH ( 10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH = 10- 11 and then extracted with EtOAc (2 x 50 m L) . The combined organic layers were washed with brine ( 10 mL), d ried by anhydrous Na₂S0₄, and then concentrated . The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (300 mg, yield : 87%); m/z (ES+) : 234 [M + H] ⁺ .

Intermediate 100

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-methoxy-5-rtrifluoromethvnphenvnethvn-/V-methyl-6-

To a solution of triphosgene (129 mg, 0.4 mmol) in EtOAc (5 mL) at 0 °C was added solution of Intermediate 54 (300 mg, 1 mmol), DMAP (11 mg, 0.01 mmol) and TEA (293 mg, 2.9 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-methoxy-5-(trifluoromethyl)phenyl)-N-methylethanamine (300 mg, 1.2 mmol) in EtOAc (10 mL) and TEA (293 mg, 2.9 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (450 mg, yield : 66%) as yellow solid; m/z (ES+) : 570 [M + H] ⁺ .

Intermediate 101

(S)-/V-((S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2- sulfinamide

To a solution of (S)-N-((S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)ethyl)-2-methyl propane-2-sulfinamide (350 mg, 1.12 mmol) in THF (10 mL) under N₂ atmosphere, was dropwise added LHMDS (2.24 mL, 1 M in THF, 2.24 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (240 mg, 1.69 mmol). The mixture was stirred at rt for another 3 h and quenched with water at 0 °C. The resulting mixture was extracted with EtOAc (2 x 40 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography(PE/EtOAc=5/l to 2/1) to give the title compound (270 mg, yield : 74%); m/z (ES+) : 326 [M + H] ⁺ .

Intermediate 102

(S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 101 (270 mg, 0.83 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (10 mL), dried by anhydrous Na₂S0₄, and then concentrated to give the title compound (100 mg, yield : 54.5%); m/z (ES+) : 222 [M + H] ⁺ .

Intermediate 103

riS,8aS^')-7,7-diallyl-/V-rrS^')-l-r3-fluoro-5-rtrifluoromethvnphenvnethvn-/V-methyl-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)-/V-methylethanamine (100 mg, 0.45 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (70 mg, yield : 28%) as yellow solid; m/z (ES+) : 558 [M+H] ⁺ .

Intermediate 104

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-fluoro-5-rtrifluoromethvnphenvnethvn-/V-methyl-6- oxo-l-o-tolylhexahvdropyrrolor i ,2-a1pyrazine-2(l/-/)-ca rboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-fluoro-5-(trifluoromethyl)phenyl)-N-methylethanamine (100 mg, 0.45 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (71 mg, yield : 29%) as yellow solid; m/z (ES+) : 558 [M+H] ⁺ .

Intermediate 105

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-fluoro-5-rtrifluoromethvnphenvnallvn-/V-methyl-6-oxo- -o-tolylhexahydropyrrolo[ l,2-alpyrazine-2(l/-/)-ca rboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-fluoro-5-(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (100 mg, 0.43 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.96 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (84 mg, yield : 42%) as yellow solid; m/z (ES+) : 570 [M + H] ⁺ .

Intermediate 106 (S)-/V-((R)-l-(3-hvdroxy-5-(trifluoromethyl)phenyl)allyl)-/V,2-dim

sulfinamide

To a solution of (S)-/V,2-dimethyl-/V-((R)-l-(3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan- 2-yl)-5-(trifluoromethyl)phenyl)allyl)propane-2-sulfinamide (800 mg, 1.8 mmol) and NaOH (144 mg, 3.6 mmol) in THF (10 mL), was added H₂0₂ (122 mg, 3.6 mmol) at 0 °C. The reaction mixture was allowed to warm to room tempraure and stirred for 2 h. After quenched with water, the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄. and then concentrated to give the title compound (500 mg, yield : 83%); m/z (ES+) : 336 [M + H] ⁺ .

Intermediate 107

(S)-/V-((R)-l-(3-methoxy-5-(trifluoromethyl)phenyl)allyl)-N,2-dimethylpropane-2- sulfinamide

To a solution of Intermediate 106 (500 mg, 1.49 mmol) in anhydrous THF (10 mL) under N₂ atmosphere was added K₂C0₃ (414 mg, 2.98 mmol) and Mel (317 mg, 2.23 mmol). The reaction mixture was stirred for 2 h and then quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and concentrated to give the title compound (400 mg, yield : 76.9%); m/z (ES+) : 350 [M + H] ⁺ .

Intermediate 108

(R)-l-(3-methoxy-5-(trifluoromethyl)phenyl)-/V-methylprop-2-en-l-amine

A solution of Intermediate 107 (400 mg, 1.15 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (10 mL), dried by Na₂S0₄, and then concentrated. The residue was purified by silica gel chromatography (DCM/MeOH=20/l to 10/1) to give the title compound (200 mg, yield : 71%); m/z (ES+) : 246 [M + H] ⁺ . Intermediate 109

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-methoxy-5-rtrifluoromethvnphenvnallvn-/V-methyl-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-methoxy-5-(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (104 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (60 mg, yield : 32.1%) as yellow solid; m/z (ES+) : 582 [M + H] ⁺ . Intermediate 110

-2-methyl-/V-(3-(trifluoromethyl) benzyl idene)propane-2-su If inamide

To a mixture of 3-(trifluoromethyl)benzaldehyde (5 g, 28.7 mmol) and (S)-2- methylpropane-2-sulfinamide (4.17 g, 34.4 mmol) in DCM (50 ml) at 0 °C, was drop wise added Ti(0-iPr)₄ (12 g, 43 mmol) under N₂ atmosphere. After stirring for 20 h at room temperature, the reaction mixture was poured into water (100 mL) with vigorous stirring. The precipitate was filtered off and the filtrate was extracted with DCM (2 x 150 mL). The combined organic layers were washed with brine (100 mL), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (7 g, yield : 88%); m/z (ES+) : 278 [M + H] ⁺ .

Intermediate 111

-2-methyl-/V-((R)-l-(3-(trifluoromethyl)phenyl)allyl)propane-2-sulfinamide

To a solution of Intermediate 110 (7 g, 25.2 mmol) in DCM (70 mL) was drop wise added vinylmagnesium bromide (50.4 mL, 1M in THF, 50.4 mmol) at - 60 °C. The reaction mixture was stirred at room temperature for 5 h and then poured into saturated aqueous NH₄CI solution. The resulting mixture was extracted with DCM (2 x 100 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (1.7 g, yield : 22%); m/z (ES+) : 306 [M + H] ⁺ .

Intermediate 112

yl-/V-((R)-l-(3-(trifluoromethyl)phenyl)allyl)propane-2-sulfinamide

To a solution of Intermediate 111 (1.7 g, 5.6 mmol) in THF (20 mL) under N₂

atmosphere was added LiHMDS (11.2 mL, 1 M in THF, 11.2 mmol) dropwisely at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (1.5 g, 10.5 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 100 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (1.5 g, yield : 84%); m/z (ES+) : 320 [M + H] ⁺ .

Intermediate 113

(R)-l-(3,5-bis(trifluoromethyl)phenyl)-/V-methylprop-2-en-l-amine

A solution of Intermediate 112 (1.5 g, 4.7 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (10 mL), dried by Na₂S0₄, and then concentrated to give the title compound (500 mg, yield :49%); m/z (ES+) : 216 [M+H] ⁺ .

Intermediate 114

f lS.8aSV7.7-diallyl-yv-methyl-6-oxo-l-o-tolyl-yv-ffRVl-f3-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3,5-bis(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (104 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-TLC to give the title compound (50 mg, yield : 28%) as yellow solid; m/z (ES+) : 552 [M + H] ⁺ .

Intermediate 115

(S)-/V,2-dimethyl-/V-((R)-l-(3-methyl-5-(trifluoromethyl)phenyl)allyl)propane-2- sulfinamide

CF₃

To a solution of (S)-2-methyl-N-((R)-l-(3-methyl-5-(tnfluoromethyl)phenyl)allyl) propane-2-sulfinamide (400 mg, 1.25 mmol) in THF (10 mL) under N₂ atmosphere was dropwise added LiHMDS (1.9 ml, 1 M in THF, 1.9 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (712 mg, 32 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 100 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (300 mg, yield : 75%); m/z (ES+) : 334 [M + H] ⁺ .

Intermediate 116

(R)-/V-methyl-l-(3-methyl-5-(trifluoromethyl) phenyl) prop-2-en-l -a mine

A solution of Intermediate 115 (300 mg, 0.9 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 30 mL). The combined organic layers were washed with brine (10 mL), dried by Na₂S0₄ and then concentrated to give the title compound (176 mg, yield : 85%) ; m/z (ES+) : 230 [M + H] ⁺ . Intermediate 117

riS,8aSV7,7-diallyl-/V-methyl-/V-rrR')-l-r3-methyl-5-rtrifluoromethvnphenvnallvn-6-

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-N-methyl-l-(3-methyl-5-(trifluoromethyl)phenyl)prop-2-en-l-amine (100 mg, 0.44 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (74 mg, yield : 37%) as yellow solid; m/z (ES+) : 566 [M + H] ⁺ .

Intermediate 118

-bromo-3-(d if luoromethyl)-5-(trifluoromethyl) benzene

To a solution of 3-bromo-5-(trifluoromethyl)benzaldehyde (5.4 g, 21 mmol) in DCM (50 ml_) at 0 °C was added DAST (4.8 g, 30 mmol). The mixture was stirred for 1.5 h and quenched with saturated aq. NaHC03 solution. The resulting mixture was extracted with DCM (2 x 50 ml_) and dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=20/l to 5/1) to give the title compound (1.3 g, yield : 22%).

Intermediate 119

l-(difluoromethyl)-3-(trifluoromethyl)-5-viny I benzene

A mixture of Intermediate 118 (1.3 g, 4.7 mmol), tributyl(vinyl)tin (1.9 mg, 5.2 mmol) and Pd(dppf)CI₂ (342 mg, 0.47 mmol) in dioxane (15 ml_) was stirred under N₂ atmosphere at 110°C for 75 min. The reaction was concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=20/l to 5/1) to give the title compound (800 mg, yield : 80%).

Intermediate 120

3-(difluoromethyl)-5-(trifluoromethyl)benzaldehvde

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 119 (800 mg, 3.6 mmol) in DCM (30 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of PPh₃ (1 g, 3.8 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the mixture was extracted with DCM (2 x 30 mL). The organic layer was washed with brine (2 x 10 mL), dried over anhydrous Na₂S0₄ and then concentrated in vacuum. The residue was purified by silica gel chromatography (PE/EtOAc=20/l to 5/1) to give the title compound (800 mg, yield : 98%). Intermediate 121

To a mixture of Intermediate 120 (800 mg, 3.6 mmol) and (S)-2-methylpropane-2- sulfinamide (480 mg, 4 mmol) in DCM (20 ml) at 0 °C, was drop wise added Ti(0-iPr)₄ (1.7 g, 6 mmol) under N₂ atmosphere. After stirring for 20 h at room temperature, the reaction mixture was poured into water (100 mL) with vigorous stirring. The precipitate was filtered off and the filtrate was extracted with DCM (2 x 50 mL). The compbined organic layers were washed with brine (30 mL), dried over anhydrous MgS0₄, and then concentrated . The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (800 mg, yield : 66%); m/z (ES+) : 328 [M + H] ⁺ .

Intermediate 122

(S)-/V-((R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2- sulfinamide

To a solution of Intermediate 121 (800 mg, 2.4 mmol) in DCM (20 mL) was drop wise added methyl magnesium bromide (3.5 mL, 1 M in THF, 3.5 mmol) at - 60 °C. The reaction mixture was stirred at room temperature for 5 h and then poured into saturated aqueous NH₄CI solution. The resulting mixture was extracted with DCM (2 x 100 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (600 mg, yield : 71%); m/z (ES+) :

344 [M + H] ⁺ .

Intermediate 123

(S)-/V-((R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane- -sulfinamide

To a solution of Intermediate 122 (850 mg, 2.5 mmol) in THF (20 ml_) under N₂ atmosphere was dropwise added LHMDS (5 ml_, 1 M in THF, 5 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (0.62 ml, 9.9 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 50 ml_). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (620 mg, yield : 73%); m/z (ES+) : 358 [M + H] ⁺ .

Intermediate 124

(R)-l-(3-(difluoromethyl)-5-(trifluoromethyl) phenyl )-/V-methylethana mine

A solution of Intermediate 123 (620 mg, 1.7 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutrilized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na₂S0₄, and then concentrated to give the title compound (340 mg, yield : 76%); m/z (ES+) : 254 [M + H] ⁺ .

Intermediate 125

riS,8aSV7,7-diallyl-/V-rrRVl-r3-rdifluoromethvn-5-rtrifluoromethvnphenvnethvn-/V- methyl-6-oxo-l-o-tolylhexahvdropyrrolor i,2-a1pyrazine-2(l/-/)-carboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-(difluoromethyl)-5-(trifluoromethyl)phenyl)-N-methylethanamine (113 mg, 0.42 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (70 mg, yield : 32%) as yellow solid; m/z (ES+) : 590 [M + H] ⁺ .

Intermediate 126

mo-5-(trifluoromethyl)phenyl)allyl)-2-methylpropane-2-sulfinamide

To a solution of (S)-/V-(3-bromo-5-(trifluoromethyl)benzylidene)-2-methylpropane-2- sulfinamide (20 g, 56.1 mmol) in DCM (300 mL) was drop wise added vinylmagnesium bromide (84 mL, 1 M in THF, 84 mmol) at - 60 °C. The reaction mixture was stirred at room temperature for 5 h and poured into aqueous NH₄CI solution. The resulting mixture was extracted with DCM (2 x 100 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (12 g, yield : 56%); m/z (ES+) : 384 [M + H] ⁺ . Intermediate 127

(S)-/V-((R)-l-(3-bromo-5-(trifluoromethyl)phenyl)allyl)-/V,2-dimethylpropane-2- sulfinamide

To a solution of Intermediate 126 (12 g, 31.2 mmol) in THF (100 mL) under N₂ atmosphere was dropwise added LHMDS (5 mL, 1 M in THF, 50 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (670 mg, 46.8 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 xlOO mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography(PE/EtOAc=5/l to 2/1) to give the title compound (7 g, yield : 60%); m/z (ES+) : 398 [M + H] ⁺ .

Intermediate 128

rSVA/,2-dimethyl-A/-rrR^')-l-r3-r4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-vn-5-

To a solution of Intermediate 127 (5 g, 12.5 mmol), Bis(pinacolato)diboron (3.8 g, 15 mmol), K₂C0₃ (3.5 g, 25 mmol) in 60 mL of THF/H₂0 (5 : 1) under N₂ atmosphere was added Pd(dppf)CI₂ (1 g, 1.25 mmol). The reaction was stirred for 5 h at 80 °C. After cooled down to room teperature, the reaction was quenched with water and then extracted with EtOAc (2 x 50 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (900 mg, yield : 45%); m/z (ES+) : 446 [M + H] ⁺ .

Intermediate 129

-l-(3-chloro-5-(trifluoromethyl)phenyl)-/V-methylprop-2-en-l-amine

To a solution of Intermediate 128 (800 mg, 1.8 mmol) in 30 mL of MeOH/H20 (10 : 1), was added CuCI₂ (1.2 g, 9 mmol). The reaction was stirred at 80 °C for 10 h and then quenched with water. The resulting mixture was extracted with EtOAc (2 x 50 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography

(PE/EtOAc=5/l to 2/1) to give the title compound (200 mg, yield : 45%); m/z (ES+) : 250 [M + H] ⁺ .

Intermediate 130

riS.8aS^')-7.7-diallyl-/V-rrR^')-l-r3-chloro-5-rtrifluoromethvnphenvnallvn-/V-methyl-6-oxo- -o-tolylhexahydropyrrolo[ l,2-alpyrazine-2(l/-/)-ca rboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-chloro-5-(trifluoromethyl)phenyl)-N-methylprop-2-en-l-amine (100 mg, 0.40 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (80 mg, yield : 40%) as yellow solid; m/z (ES+) : 586 [M + H] ⁺ .

Intermediate 131

(R)-/V-(3,5-bis(trifluoromethyl) benzyl idene)-2-methylpropane-2-sulfinamide

To a mixture of 3,5-bis(trifluoromethyl)benzaldehyde (5 g, 20.7 mmol) and (R)-2- methylpropane-2-sulfinamide (3.3 g, 26.9 mmol) in DCM (50 ml) at 0 °C, was drop wise added Ti(0-iPr)₄ (5.9 g, 24.8 mmol) under N₂ atmosphere. After stirring for 20 h at room temperature, the reaction mixture was poured into water (100 ml_) with vigorous stirring. The precipitate was filtered off and the filtrate was extracted with DCM (2 x 100 ml_). The combined organic layers were washed with brine (100 ml_), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (5.5 g, yield : 78%); m/z (ES+) : 346 [M + H] ⁺ .

Intermediate 132

-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-2-methylpropane-2-sulfinamide

To a solution of Intermediate 131 (5.0 g, 14.5 mmol) in DCM (50 ml_) was drop wise added methyl magnesium bromide (6.3 ml_, 3 M in THF, 19 mmol) at - 60 °C. After stirring for 5 h at room temperature, the reaction was poured into saturated aqueous NH₄CI solution and extracted with DCM (2 x 100 ml_). The organic combined layers were washed with brine (50 ml_), dried over anhydrous MgS0₄, and then concentrated. The residue was purified by silica gel chromatography (PE/EtOAc=5/l to 2/1) to give the title compound (3.5 g, yield : 67%); m/z (ES+) : 362 [M + H] ⁺ .

Intermediate 133

-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2-sulfinamide

To a solution of Intermediate 132 (2.0 g, 5.5 mmol) in THF (30 ml_) under N₂ atmosphere was dropwise added LiHMDS (7.2 ml_, 1 M in THF, 7.2 mmol) at -60 °C. The reaction was stirred for 30 min at -60 °C followed by addition of Mel (1.6 g, 11 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 60 ml_). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated under reduced presure. The residue was purified by silica gel chromatography(PE/EtOAc=5/l to 2/1) to give the title compound (1.3 g, yield : 65%); m/z (ES+) : 376 [M + H] ⁺ .

Intermediate 134 (S)-l-(3,5-bis(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 133 (1.3 g, 3.47 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutralized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na₂S0₄, and then concentrated to give the title compound (0.7 g, yield : 75%); m/z (ES+) : 272 [M + H] ⁺ .

Intermediate 135

riS,8aS^')-7,7-diallyl-/V-rrS^')-l-r3,5-bisrtrifluoromethvnphenvnethvn-/V-methyl-6-oxo-l- -tolylhexahvdropyrrolor i,2-a1pyrazine-2(l/-/)-carboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (S)-l-(3,5-bis(trifluoromethyl)phenyl)-N-methylethanamine (147 mg, 0.54 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (40 mg, yield : 17%) as yellow solid; m/z (ES+) : 608 [M + H] ⁺ .

Intermediate 136

riS.SaSVdimethyl 2-fmethylff RVl-f3-methyl-5-

(trifluoromethyl)phenyl)ethyl)ca rbamoyl)-6-oxo-l-o-tolylhexahyd ropy rrolof 1,2- alpyrazine-7,7(6/-/)-dicarboxylate

To a solution of (lS,8aS)-/V-methyl-/V-((R)-l-(3-methyl-5-(tnfluoromethyl)phenyl)ethyl) -6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)-carboxamide (350 mg, 0.74 mmol) in anhydrous THF (20 mL) under N₂ atmosphere was added LHMDS (4.43 mL, 1 M in THF, 4.43 mmol) at -60 °C. The reaction was stirred for 30 min followed by addition of methyl carbonochloridate (174 mg, 1.85 mmol). After stirring for another 3 h at room temperature. The reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 30 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel

chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (200 mg, yield : 46%); m/z (ES+) : 590 [M + H] ⁺ .

Intermediate 137

(lS,8aS)-di methyl 2-(((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)(methyl)carbamoyl)- -oxo-l-o-tolylhexahydropyrrolo[ l,2-alpyrazine-7,7(6/-/)-dicarboxylate

To a solution of (lS,8aS)-N-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-N-methyl-6- oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(lH)-carboxamide (300 mg, 0.57 mmol) in anhydrous THF (20 mL) under N₂ atmosphere was added LiHMDS (2.3 mL, 1 M in THF, 2.3 mmol) at -60 °C. The reaction was stirred for 30 min followed by addition of methyl carbonochloridate (134 mg, 1.43 mmol). After stirring for another 3 h at room

temperature. The reaction was quenched with water at 0 °C and then extracted with EA (2 x 50 mL) . The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (166 mg, yield : 45.3%); m/z (ES+) : 644 [M + H] ⁺ .

Intermediate 138 (lS,8aS)-di methyl 2-(((R)-l-(3,5-bis(tnfluoromethvnphenvnethvn(methyl^')carbamoyl^')- -oxo-l-o-tolylhexahvdropyrrolor i,2-a1pyrazine-7,7(6/-/)-dicarboxylate

To a solution of (lS,8aS)-N-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-N-methyl- 6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(lH)-carboxamide (300 mg, 0.61 mmol) in anhydrous THF (20 mL) under N₂ atmosphere was added LiHMDS (2.3 mL, 1 M in THF, 2.3 mmol) at -60 °C. The reaction was stirred for 30 min followed by addition of methyl carbonochloridate (134 mg, 1.43 mmol). After stirring for another 3 h at room temperature, the reaction was quenched with water at 0 °C and then extracted with EtOAc (2 x 30 mL). The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel

chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (220 mg , yield : 59%); m/z (ES+) : 610 [M + H] ⁺ . Intermediate 139

(S)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethylpropane-2- sulfinamide

A mixture of (S)-/V-((R)-l-(3-bromo-5-(trifluoromethyl)phenyl)ethyl)-/V,2-dimethyl propane-2-sulfinamide (1 g, 2.6 mmol), Pd(PPh₃)₂CI₂ (182 mg, 0.26 mmol) and Et₂Zn

(640 mg, 5.2 mmol) in THF (10 mL) under N₂ atmosphere was stirred at 6 °C for 16 h.

The reaction was poured into water (15 mL) and then extracted with EtOAc (2 x 30 mL).

The combined organic layers were dried over anhydrous Na₂S0₄ and then concentrated.

The residue was purified by silica gel chromatography (PE/EtOAc= 10/l to 1/1) to give the title compound (700 mg, yield : 80.3%); m/z (ES+) : 336 [M + H] ⁺ .

Intermediate 140

(R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 139 (700 mg, 2.09 mmol) in HCI/MeOH (10 mL) under N₂ atmosphere was stirred for 15 min. The reaction was neutrilized with 1 M NaOH solution to pH= 10-11 and then extracted with EtOAc (2 x 50 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous Na₂S0₄, and then concentrated to give the title compound (300 mg, yield : 62%); m/z (ES+) : 232 [M + H] ⁺ .

Intermediate 141

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of Intermediate 54 (100 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)-/V-methylethanamine (111 mg,

0.48 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (78 mg, yield : 43%) as yellow solid; m/z (ES+) : 568 [M + H] ⁺ .

Intermediate 142

(S)-/V,2-dimethyl-/V-((R)-l-(3-(prop-l-en-2-yl)-5-(trifluoromethyl)phenyl)ethyl)propane- 2-sulfinamide

To a solution of Intermediate 74 (1.8 g, 4.66 mmol) in THF (20 mL) under N₂ atmosphere was added Pd(PPh₃)₄ (100 mg , 0.1 mmol), 4,4,5,5-tetramethyl-2-(prop-l- en-2-yl)-l,3,2-dioxaborolane (1 g , 6 mmol). The reaction was refluxed for 4 h and then quenched with water. The resulting mixture was extracted with EtOAc (2 x 100 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc= 10/1 to 1/1) to give the title compound (1.4 g, yield : 86%); m/z (ES+) : 348 [M + H] ⁺ .

Intermediate 143

(S)-/V-((R)-l-(3-isobrobyl-5-(trifluoromethyl)bhenyl)ethyl)-/V,2-di methyl brobane-2- sulfinamide

To a solution of Intermediate 142 (1.4 g, 4 mmol) in MeOH (20 mL) under N₂ atmosphere was added Pd/C (0.2 g). The resulting mixture was purged with N2 twices and then stirred under hydrogen atmosphere (50 psi) for 24 h at room temperature. The mixture was filtered and the filtrate was concentrated in high vacuum. The residue was purified by silica gel chromatography (PE/EtOAc= 5/1 to 1/1) to give the title compound (1.2 g, yield : 85%); m/z (ES+) : 350[M + H] ⁺ . Intermediate 144

(R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)-/V-methylethanamine

A solution of Intermediate 143 (1.2 g, 3.44 mmol) in HCI/MeOH (2 N, 10 mL) was stirred for 1 h under N₂ atmosphere. The reaction was neutralized with 1 N NaOH to pH = 10-11 and then extracted with EtOAc (2 x 20 mL). The organic layers were dried over anhydrous Na₂S0₄ and then concentrated in high vacuum to give the title compound (0.8 g, yield : 95%) which used directly in the next step; m/z (ES+) : 246 [M + H] ⁺ .

Intermediate 145

riS,8aS^')-7,7-diallyl-/V-rrR^')-l-r3-isobropyl-5-rtrifluoromethvnphenvnethvn-/V-methyl-6- oxo-l-o-tolylhexahydropyrrolo[ l ,2-alpyrazine-2(l/-/)-ca rboxamide

To a solution of triphosgene (72 mg, 0.242 mmol) in EtOAc (2 mL) at 0 °C was added solution of (lS,8aS)-7,7-diallyl-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazin-6(7/-/)-one (150 mg, 0.484 mmol), DMAP (6.2 mg, 0.05 mmol) and TEA (151 mg, 1.5 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-isopropyl-5- (trifluoromethyl)phenyl)-/V-methylethanamine (142 mg, 0.58 mmol) in EtOAc (10 mL) and TEA (151 mg, 1.5 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (100 mg, yield : 36%) as yellow solid; m/z (ES+) : 582 [M + H] ⁺ .

Compounds described in the examples below were obtained as amorphous compounds. Example 1 : Compound 1

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methylphenyl)-6-oxooctahyd ropy rrolo [ l ,2-alpiperazine-2-carboxamide

(enantiomer 1, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

Triphosgene (27.3 mg, 0.09 mmol) was dissolved in EtOAc (1 mL) at 0 °C. A solution l-(2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazin-6-one hydrochloride salt

(Intermediate 24, 60 mg, 0.23 mmol) and TEA (110 mL, 0.8 mmol) in EtOAc (2 mL), was added. The reaction mixture was stirred at 0°C for 1.5 h, then a solution of

Intermediate 3 (43.5 mg, 0.32 mmol) and TEA (30 mL) in EtOAc (2 mL), was added. The reaction mixture was stirred 2 h at room temperature. Water (20 mL) was added followed by EtOAc (20 ml_). The organic layer was dried over Na₂S0₄, filtered and evaporated under vacuo to give a yellow oil (110 mg) which was subjected to chiral preparative HPLC. Two fractions were obtained. After evaporation two products were obtained: enantiomer 1 (Compound 1) and enantiomer 2 (Compound 2, see

experimental below). Enantiomer 1 (white solid, 19.4 mg). Chiral HPLC: column

Chiralpak AD-H (25 x 0.46 cm), 5μ, Mobile phase: n-Hexane/2-Propanol 85/15 v/v, Flow rate: 1 mL/min, Detection: DAD at 220 nm. Rt=10.6 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.32 (d, 7=6.8 Hz, IH), 7.18 (m, 3H), 6.86 (s, IH), 6.52 (s, 2H), 4.39 (m, 2H), 4.15 (m, IH), 4.08 (d,7=9.8 Hz, IH), 3.70 (m, 7=9.5 Hz, IH), 3.35 (m, IH), 3.12 (td, 7=12.4, 3.1 Hz, IH), 2.93 (td, 7=12.0, 3.3 Hz, IH), 2.83 (s, 3H), 2.55 (s, 3H), 2.41 (m, IH), 2.34 (m, IH), 2.22 (s, 6H), 1.84 (m, IH), 1.70 (d, 7=7.6 Hz, IH).

Example 2: Compound 2

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methylphenyl)-6-oxooctahyd ropy rrolo [l,2-alpiperazine-2-carboxamide

(enantiomer 2, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

After evaporation of fraction collected from chiral preparative HPLC of the above described experimental, Compound 2 was obtained (white solid, 14.8 mg). Chiral HPLC, Chiralpak AD-H column (25 x 0.46 cm), 5μ mobile phase: n-Hexane/2-Propanol 85/15 v/v, Flow rate: 1 mL/min. Detection: DAD at 220 nm. Rt= 21.5 min. *H NMR (500 MHz, CDCI₃) δ ppm 7.32 (d, 7=6.8Hz, IH), 7.18 (m, 3H), 6.86 (s, IH), 6.52 (s, 2H), 4.39 (m, 2H), 4.15 (m, IH), 4.08 (d,7=9.8Hz, IH), 3.70 (m, 7=9.5Hz, IH), 3.35 (m, IH), 3.12 (td, 7=12.4, 3.1Hz, IH), 2.93 (td, 7=12.0, 3.3Hz, IH), 2.83 (s, 3H), 2.55 (s, 3H), 2.41 (m, IH), 2.34 (m, IH), 2.22 (s, 6H), 1.84 (m, IH), 1.70 (d,7=7.6Hz, IH).

Example 3: Compound 3

N--{ 3-fluoro-5-(trifluoromethyl) phenyl] methyl -N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(enantiomer 1, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

Triphosgene (27.3 mg, 0.09 mmol) was dissolved in ETOAc (1 mL) at 0 °C. A solution of l-(2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazin-6-one hydrochloride salt

(Intermediate 24, 60 mg, 0.23 mmol) and TEA (110 mL, 0.8 mmol) in EtOAc (2 mL), was added. The reaction mixture was stirred at 0°C for 1.5 h, then a solution of {[3- fluoro-5-(trifluoromethyl)phenyl]methyl}(methyl)amine (intermediate 4, 66.3 mg, 0.32 mmol) and TEA (30 mL) in EtOAc (2 mL), was added. The reaction mixture was stirred 2 h at room temperature. Water (20 mL) was added followed by EtOAc (20 mL). The organic layer was dried over Na₂S0₄, filtered and evaporated in vacuo to give a yellow oil (130 mg) which was subjected to chiral preparative HPLC. Two fractions were obtained. After evaporation two products were obtained : enantiomer 1 (Compound 3) and enantiomer 2 (Compound 4, see experimental below). Compound 3 : white foam, 33.8 mg. Chiral HPLC, Chiralpak AD-H column (25 x 0.46 cm), 5μ, Mobile phase: n- Hexane/2-Propanol 85/15 v/v, Flow rate: 0.8 mL/min; Detection : DAD at 220 nm.

Rt= 12.8 min. m/z (ES+) : 464.2 [M + H] ⁺ . ^JH NMR (500 MHz, CDCI₃) δ ppm 7.28 (m, IH), 7.19 (m, 4H), 7.03 (s, IH), 6.57 (d, .7=8.8Hz, IH), 4.66 (d, J= 15.4Hz, IH), 4.23 (d, .7= 15.7Hz, IH), 4.18 (dt, .7= 13.0, 2.7Hz, IH), 4.08 (d, J= 10.0Hz, IH), 3.73 (dt, 3=9.7, 7.4Hz, IH), 3.35 (dt, .7= 12.2, 2.8Hz, IH), 3.14 (td, .7= 12.5, 2.7Hz, IH), 2.95 (m, 4H), 2.53 (s, 3H), 2.44 (m, IH), 2.36 (m, IH), 1.87 (m, IH), 1.70 (m, IH).

Example 4 : Compound 4

N--{ 3-fluoro-5-(trifluoromethyl) phenyl] methyl -N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-alpiperazine-2-carboxamide

(enantiomer 2, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

After evaporation of fraction collected from chiral preparative HPLC of the above described experimental, compound 4 was obtained (white foam, 34.8 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2-Propanol 85/15 v/v, Flow rate: 0.8 mL/min. Detection: DAD at 220 nm. Rt=15.8 min. m/z (ES+): 464.2 [M + H] ⁺ . ^JH NMR (500 MHz, CDCI₃) δ ppm 7.28 (m, 1H), 7.19 (m, 4H), 7.03 (s, 1H), 6.57 (d, .7=8.8Hz, 1H), 4.66 (d, -7=15.4Hz, 1H), 4.23 (d, -7=15.7Hz, 1H), 4.18 (dt,

.7=13.0, 2.7Hz, 1H), 4.08 (d, -7=10. OHz, 1H), 3.73 (dt, -7=9.7, 7.4Hz, 1H), 3.35 (dt, -7=12.2, 2.8Hz, 1H), 3.14 (td, -7=12.5, 2.7Hz, 1H), 2.95 (m, 4H), 2.53 (s, 3H), 2.44 (m, 1H), 2.36 (m, 1H), 1.87 (m, 1H), 1.70 (m, 1H).

Example 5: Compound 5

N-methyl-l-(2-methylphenyl)-6-oxo-N-- r3-(trifluoromethyl)phenyl1 methyl -Octa hydro pyrrolori,2-a1piperazine-2-carboxamide

(enantiomer 1, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

Triphosgene (27.3 mg, 0.09 mmol) was dissolved in ETOAc (1 mL) at 0 °C. A solution of l-(2-methylphenyl)-octahydropyrrolo[l,2-a]piperazin-6-one hydrochloride salt

(Intermediate 24, 60 mg, 0.23 mmol) and TEA (110 mL, 0.8 mmol) in EtOAc (2 mL), was added. The reaction mixture was stirred at 0°C for 1.5h, then a solution of methyl({[3-(trifluoromethyl)phenyl]methyl})amine (Intermediate 2, 60 mg, 0.32 mmol) and TEA (30 mL) in EtOAc (2 mL), was added. The reaction mixture was stirred 2h at room temperature. Water (20 ml_) was added followed by EtOAc (20 ml_). The organic layer was dried over Na₂S0₄, filtered and evaporated under vacuo to give a yellow oil (130 mg) which was subjected to chiral preparative HPLC. Two fractions were obtained. After evaporation two products were obtained: enantiomer 1 (Compound 5) and enantiomer 2 (Compound 6, see experimental below). Compound 5 (white solid, 26 mg): chiral HPLC, Chiralpak AD-H column (25 x 0.46 cm), 5μ, Mobile phase: n- Hexane/2-Propanol 85/15 v/v, Flow rate: 0.8 mL/min; Detection: DAD at 220 nm.

Rt=17.9 min. m/z (ES+): 446.2 [M + H]^{+ J}H NMR (500 MHz, CDCI₃) δ ppm 7.47 (d, .7=7.6 Hz, IH), 7.21 (m, 6H), 6.88 (d, J=7.8Hz, IH), 4.60 (d, J=15.4Hz, IH), 4.34 (d,

.7=15.2Hz, IH), 4.17 (d, .7=13.0Hz, IH), 4.08 (d, .7=10. OHz, IH), 3.73 (m, IH), 3.34 (d, .7=12.0Hz, IH), 3.13 (m, IH), 2.95 (m, 4H), 2.54 (s, 3H), 2.40 (m, 2H), 1.87 (m, IH), 1.69 (m, IH).

Example 6: Compound 6

N-methyl-l-(2-methylphenyl)-6-oxo-N-- [3-(trifluoromethyl)phenyllmethyl -Octahydro pyrrolo[l,2-alpiperazine-2-carboxamide

(enantiomer 2, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

After evaporation of fraction collected from chiral preparative HPLC of the above described experimental, Compound 6 was obtained (white solid, 33 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2-Propanol 85/15 v/v, Flow rate: 0.8 mL/min. Detection: DAD at 220 nm. Rt=23.6 min. m/z (ES+): 446.2 [M + H]^{+ J}H NMR (500 MHz, CDCL₃) δ ppm 7.47 (d, .7=7.6 Hz, IH), 7.21 (m, 6H), 6.88 (d, .7=7.8Hz, IH), 4.60 (d, J=15.4Hz, IH), 4.34 (d, J=15.2Hz, IH), 4.17 (d, .7=13. OHz, IH), 4.08 (d, .7=10.0Hz, IH), 3.73 (m, IH), 3.34 (d, .7=12. OHz, IH), 3.13 (m, IH), 2.95 (m, 4H), 2.54 (s, 3H), 2.40 (m, 2H), 1.87 (m, IH), 1.69 (m, IH).

Example 7: Compound 7

N--r3,5-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)-7-oxo-octa hydro- lH-pyrrolori,2-airi,41diazepine-2-carboxamide (diastereomeric mixture)

Triphosgene (12 mg) was dissolved in ETOAc (0.5 ml_) at 0°C. A solution of l-(2- methylphenyl)-octahydro-lH-pyrrolo[l,2-a][l,4]diazepin-7-one (Intermediate 8, 20 mg, 0.08 mmol) and TEA (15 ml_, 0.11 mmol) in EtOAc (0.5 ml_), was added. The reaction mixture was stirred at room temperature for 2h, then a solution of {[3,5- bis(trifluoromethyl)phenyl]methyl}(methyl)amine (Intermediate 18, 29 mg, 0.1 mmol) and TEA (15 ml_, 0.11 mmol) in EtOAc (0.5 ml_), was added. The reaction mixture was stirred 4h at room temperature. NaOH 1M and EtOAc were added. The organic layer was dried over Na₂S0₄, filtered and evaporated under vacuo to give a yellow oil that was purified on biotage KP-Sil cartridge (CH/EtOAc and then DCM/MeOH as eluent). Collected fractions were evaporated to give a yellow oil (11 mg). ¹H NMR (500 MHz, CDCI₃) δ ppm 7.78 (s, 1H), 7.64 (s, 2H), 5.33 (d, .7=3.4 Hz, 1H), 4.53 (m, 1H), 4.47 (s, 2H), 4.01 (ddd, .7=13.7, 8.3, 3.9Hz, 1H), 3.62 (m, 1H), 3.32 (ddd, .7=13.9, 7.8, 3.4 Hz, 1H), 3.26 (ddd, .7=14.9, 6.8, 3.7 Hz, 1H), 2.77 (s, 3H), 2.38 (d, .7=6.6 Hz, 3H), 2.20 (m, 2H), 2.10 (m, 1H), 1.98 (m, 1H), 1.87 (m, 1H), 1.70 (m, 1H); UPLC-MS: Rt=1.21 min and 1.24 min; m/z (ES+): 528.3 [M + H] ⁺ .

Example 8: Compound 8

2-({ \3, 5-bis(trifluoromethyl) phenyl] methyl XmethyDcarbamoy l)-7-methyl-l -(2- methylphenyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-7-carboxylic acid

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Intermediate 19 (6 mg, 0.010 mmol) was dissolved in a mixture of THF/H₂0/MeOH (0.2 mL each) and LiOH-H₂0 (1.2 mg, 0.02 mmol) was added. The mixture was heated at 60°C for 2h, then the solution was concentrated and DCM and HCI 1M aq were added. The phases were separated and the organic layer was filtered through a phase separator and concentrated to give the title compound (5.8 mg). *H NMR (500 MHz, DMSO-d6) δ ppm 12.86 (br s, 1H), 7.95 (s, 1H), 7.58 (s, 2H), 7.34 (m, 1H), 7.09 (m, 3H), 4.58 (d, 1H), 4.48 (d, 1H), 4.12 (d, 1H), 3.88 (m, 1H), 3.76 (m, 1H), 3.48 (m, 1H), 3.23 (m, 1H), 2.87 (s, 3H), 2.75 (m, 1H), 2.00 (m, 2H), 1.60 (m, 3H), 1.23 (s, 3H). UPLC-MS: Rt= 1.20 min; m/z (ES+): 572 [M + H] ⁺ .

Example 9: Compound 9 and Example 10: Compound 10

N-r(lR)-l-r3,5-bis(trifluoromethyl^')phenyl1ethyl1-N-methyl-l-(2-methylphenyl^')-6-oxo- octahvdropyrrolori,2-a1 piperazine-2-carboxamide:

Example 9: Compound 9

flS.8aSVN-rflRVl-r3.5-bisftrifluoromethvnphenvnethvn-N-methyl-l-f2- methylphenyl)-6-oxo-octahydropyrrolo|^'l,2-a1 piperazine-2-carboxamide

(enantiomer 1, single isomer with ANTI configuration at Cl-C8a)

Triphosgene (204.45 mg, 0.6 mmol) was dissolved in EtOAc (10 mL), this solution was cooled at 0 °C and a solution of Intermediate 13 (480 mg, 70% purity, 1.46 mmol) and TEA (400 μί, 2.88 mmol) in EtOAc (20 mL) was added. The resulting mixture was left stirring at this temperature for 2h, then TEA (400 μί, 2.88 mmol) and Intermediate 1 (554.27 mg, 2.044 mmol) in EtOAc (20 mL) were added and the mixture was left stirring for 3h. Further 600 mg of Intermediate 1 in 10 mL of EtOAc were added and the mixture was left stirring for 36h. NaOH 1M was added to the mixture, the phases were separated and the aqueous one was extracted with EtOAc. The organic layer was dried over Na₂S0₄ and concentrated in vacuo to obtain 1.56 g of a crude which was subjected to chiral preparative HPLC. Two fractions were obtained. After evaporation two products were obtained: enantiomer 1 and enantiomer 2 (see experimental below). (lS,8aS)-N-[(lR)- l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-6-oxo- octahydropyrrolo[l,2-a] piperazine-2-carboxamide, (Enantiomer 1): (white solid, 47 mg). Chiral column: Chiralpak AS-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 80/20 v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm, Rt=10.3 min; *H NMR (400 MHz, CDCI₃) δ ppm 7.79 (s, 1H), 7.55 (s, 2H), 7.25 (d, 1H), 7.16 (m, 3H), 5.55 (q, 1H), 4.16 (dt, IH), 4.08 (d, IH), 3.74 (m, IH), 3.27 (dt, IH), 3.12 (td,lH), 2.98 (td, IH), 2.71 (s, 3H), 2.54 (s, 3H), 2.43 (m, IH), 2.34 (m, IH), 1.86 (m, IH), 1.68 (m, IH), 1.41 (d, 3H). Rt=1.24 min; m/z (ES+) 528.3 [M + H]⁺ . Example 10: Compound 10

riR,8aRVN-rriRVl-r3,5-bisrtnfluoromethvnphenyllethyll-N-methyl-l-r2- methylphenyl)-6-oxo-octahvdropyrrolori,2-a1 piperazine-2-carboxamide

(enantiomer 2, single isomer with ANTI configuration at Cl-C8a)

(lR,8aR)-N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2- methylphenyl)-6-oxo-octahydropyrrolo[l,2-a] piperazine-2-carboxamide (Enantiomer 2) (50 mg) was isolated and characterized as follows. Chiral HPLC (from the above described experimental): Chiral column Chiralpak AS-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 80/20 v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm Rt=14.7 min. ^JH NMR (500 MHz, CDCI₃)) δ ppm 7.72 (s, IH), 7.36 (s, 2H), 7.24 (d, .7=7.1 Hz, IH), 7.16 (m, 3H), 5.59 (q, .7=7.1 Hz, IH), 4.18 (dt, .7=12.6, 2.8 Hz, IH),

4.08 (d, =10.0 Hz, IH), 3.69 (dt, .7=9.7, 7.4 Hz, IH), 3.33 (m, IH), 3.13 (td, .7=12.3,

2.9 Hz, IH), 2.93 (td, .7=12.0, 3.3 Hz, IH), 2.83 (s, 3H), 2.53 (s, 3H), 2.44 (m, IH), 2.34 (m, IH), 1.85 (m, IH), 1.71 (m, IH), 1.51 (d, .7=7.3 Hz, 3H).

Example 11: Compound 11

Methyl 2-({ \3, 5-bis(trifluoromethyl) phenyl] methyl XmethyDcarbamoy l)-7-methy I- 1-(2- methylphenyl)-6-oxo-octahydropyrrolo-fl,2-a piperazine-7-carboxylate

(diastereomeric mixture with ANTI configuration at Cl-C8a)

Triphosgene (23.44 mg, 0.07 mmol) was dissolved in EtOAc (1 mL), the solution was cooled at 0°C and a solution of Intermediate 17 (52 mg, 0.172 mmol) and TEA (40 μΙ_, 0.46 mmol) in EtOAC (2 mL) was added. The resulting mixture was left stirring at this temperature for 2h, then TEA (40 μί, 0.46 mmol) and Intermediate 18 (61.91 mg, 0.240 mmol) in EtOAc (2 mL) were added and the mixture was left stirring for 3h. NaOH 1M was added to the mixture, the phases were separated and the organic layer was washed with HCI 1M and brine, dried aver Na₂S0₄ and concentrated in vacuo. The crude material was purified on SP1 (snap-NH cartridge, 11 g, CH/EtOAc 9:1 to 0:1 as eluent) to give the title compound as a white foam (70 mg).¹ NMR (500 MHz, CDCI₃) δ ppm 7.67 (s, IH), 7.29 (s, 2H), 7.19 (s, 2H), 7.10 (s, 2H), 4.62 (d, IH), 4.28 (d, IH), 4.17 (d, IH), 4.13 (dt, IH), 3.73 (s, 3H), 3.68 (m, IH), 3.30 (m, IH), 3.12 (m, IH), 2.96 (m, IH), 2.89 (s, 3H), 2.17 (m, IH), 1.69 (m, IH), 1.31 (s, 2H). UPLC-MS: Rt=1.30 min; m/z (ES+): 586 [M + H] ⁺ . Example 12: Compound 12

(enantiomer 1 of diastereoisomer 2 single isomer with ANTI configuration at Cl-C8a)

Compound 11 was separated by chiral preparative chromatography obtaining the title compound (Compound 12, 19.5 mg). Column: Chiralpak IC (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 70/30 v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm; Rt=10.3 min. ^JH NMR (500 MHz, CDCL₃) δ ppm 7.75 (s, IH), 7.37 (s, 2H), 7.27 (s, IH), 7.18 (m, 3H), 4.70 (d, .7=14.7 Hz, IH), 4.36 (d, 7=16.0 Hz, IH), 4.25 (d, 7=10.0 Hz, IH), 4.20 (m, IH), 3.81 (s, 3 H), 3.76 (m, IH), 3.38 (m, IH), 3.20 (td, 7=13.0, 3.5 Hz, IH), 3.03 (td, 7=12.0, 3.2 Hz, IH), 2.97 (s, 3H), 2.53 (s, 3H), 2.25 (dd, 7=13.7, 6.6 Hz, IH), 1.78 (dd, 7=13.2, 8.1 Hz, IH), 1.39 (s, 3 H).

Example 13: Compound 13

Methyl 2-(- r3,5-bis(trifluoromethyl)phenyl1methyl (methyl)carbamoyl)-7-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolo-f l,2-a piperazine-7-carboxylate (enantiomer 2 of diastereoisomer 1 single isomer with ANTI configuration at Cl-C8a)

Compound 11 was separated by chiral preparative chromatography obtaining the title compound (Compound 13, 5.8 mg). Column: Chiralpak IC (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 70/30 v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm; Rt=11.8 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.75 (s, IH), 7.37 (s, 2H), 7.27 (s, 2H), 7.17 (s, 2H), 4.69 (d, .7=14.9 Hz, IH), 4.36 (d, 7=15.9 Hz, 1 ), 4.18 (m, IH), 4.04 (d, 7=9.8 Hz, IH), 3.85 (q, 7=8.3 Hz, IH), 3.68 (s, 3H), 3.41 (m, IH), 3.24 (td, 7=10.8, 3.4 Hz, IH), 3.00 (dd, 7=12.2, 3.7 Hz, IH), 2.97 (s, 3H), 2.52 (s, 3H), 2.33 (dd, 7=13.0, 6.4 Hz, IH), 1.59 (m, IH), 1.51 (s, 3H).

Example 14: Compound 14

Methyl 2-({ \3, 5-bis(trifluoromethyl) phenyl] methyl XmethyDcarbamoy l)-7-methy I- 1-(2- methylphenyl)-6-oxo-octahvdropyrrolo- i,2-a piperazine-7-carboxylate

(enantiomer 2 of diastereoisomer 2 single isomer with ANTI configuration at Cl-C8a)

Compound 11 was separated by chiral preparative chromatography obtaining the title compound (Compound 14, 19 mg). Column: Chiralpak IC (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 70/30 v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm; Rt=26.4 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.74 (m, IH), 7.37 (s, 2H), 7.25 (m, 2H), 7.18 (s, 2H), 4.70 (d, 7=15.4 Hz, IH), 4.36 (d, 7=15.2 Hz, IH), 4.25 (d, 7=10.0 Hz, IH), 4.20 (m, IH), 3.81 (s, 3H), 3.76 (m, IH), 3.38 (m, IH), 3.20 (td, 7=12.4, 3.4 Hz, IH), 3.03 (td, 7=12.0, 3.2 Hz, IH), 2.97 (s, 3H), 2.53 (s, 3H), 2.25 (dd, 7=13.4, 6.8 Hz, IH), 1.78 (dd, 7=13.5, 7.2 Hz, IH), 1.39 (s, 3H). Example 15: Compound 15

Methyl 2-(-fr3,5-bis(trifluoromethyl) phenyl! methyl XmethvDcarba moyl)-7-methyl- l-(2- methylphenyl)-6-oxo-octahvdropyrrolo-f l,2-a piperazine-7-carboxylate

(enantiomer 1 of diastereoisomer 1 single isomer with ANTI configuration at Cl-C8a)

Compound 11 was separated by chiral preparative chromatography obtaining the title compound (Compound 15, 2.7 mg). Column: Chiralpak IC (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 70/30 v/v Flow rate: 0.8 mL/min. Detection: DAD at 220 nm Rt=9.1 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.75 (s, IH), 7.37 (s, 2 ), 7.28 (m, 2H), 7.17 (m, 2H), 4.69 (d, .7=15.7 Hz, IH), 4.36 (d, .7=15.7 Hz, 1H),4.17 (m, IH), 4.04 (d, .7=10.0 Hz, IH), 3.85 (q, 7=8.8 Hz, IH), 3.68 (s, 3H), 3.40 (m, IH), 3.24 (td, 7=12.5, 3.2 Hz, IH), 3.00 (dd, 7=13.0, 2.9 Hz, 2H),2.97 (s, 3H), 2.53 (m, 3H), 2.33 (dd, 7=13.2, 6.8 Hz, IH), 1.59 (d, 7=8.1 Hz, IH), 1.51 (s, 3H).

Example 16: Compound 16

Α/--Γ [3, 5-bis(trifluoromethyl) phenyl] methyl -/V-methyl-l -(2-methyl phenyl)-6-oxo- octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(racemic mixture with ANTI configuration at Cl-C8a)

Triphosgene (30.7 mg, 0.09 mmol) was dissolved in EtOAc (1 mL). The solution was cooled to 0°C and a solution of Intermediate 13 (51.8 mg, 0.22 mmol) in EtOAc (1 mL) and TEA (50 μί, 0.6 mmol) were added. The reaction mixture was stirred at this temperature for 2 h, then EtOAc (2 mL), TEA (50 μΐ) and Intermediate 18 (81 mg, 0.31 mmol) were added. The reaction was stirred at 25°C for 2h, then NaOH 1M was added and the organic layer was washed with water, dried over sodium sulphate, filtered and concentrated in vacuo to give a crude that was purified on SPl (snap cartridge, 10 g, CH/EtOAc 7:3 to DCM/MeOH 9:1 as eluent) to give the title compound (57 mg). ^JH NMR (600 MHz, DMSO- 6) δ ppm 7.93 (s, IH), 7.57 (s, 2H), 7.30 (dd, IH), 7.07 (m, 3 H), 4.55 (d, IH), 4.46 (d, IH), 3.96 (d, IH), 3.85 (dt, IH), 3.66 (dt, IH), 3.44 (dt, IH), 3.12 (m, IH), 2.86 (s, 3H), 2.73 (td, IH), 2.40 (s, 3H), 2.20 (m, 2H), 1.62 (m, IH), 1.52 (m, IH). HPLC-MS: Rt=1.25 min; m/z (ES+): 514.3 [M + H] ⁺ .

Example 17: Compound 17

A/-- r3,5-bis(trifluoromethvnphenyl1 methyl -/V-methyl-l -(2-methyl phenvn-6-oxo- octahvdropyrrolori,2-a1piperazine-2-carboxamide

(enantiomer 1, single isomer with ANTI configuration at Cl-C8a)

Separation by chiral chromatography of Compound 16, from the above described experimental, provided 20.8 mg of the title compound (enantiomer 1). ¹ NMR (500 MHz, CDCI₃) δ ppm 7.74 (s, IH), 7.37 (s, 2H), 7.26 (m, IH), 7.15 (m, 3H), 4.69 (d, IH), 4.36 (d, IH), 4.18 (dt, IH), 4.09 (d, IH), 3.73 (m, IH), 3.37 (m, IH), 3.15 (m, IH), 2.96 (s, 3H), 2.96 (m, IH), 2.53 (s, 3H), 2.44 (m, IH), 2.35 (m, IH), 1.87 (dddd, IH), 1.69 (m, IH). Chiral HPLC: Rt=15.3 min. Example 18: Compound 18

(enantiomer 2, single isomer with ANTI configuration at Cl-C8a)

Separation by chiral chromatography of Compound 16, from the above described experimental, provided 19.6 mg of the title compound (enantiomer 2). ¹ NMR (500 MHz, CDCI₃) δ ppm 7.74 (s, IH), 7.37 (s, 2H), 7.26 (m, IH), 7.16 (m, 3H), 4.69 (d, IH), 4.36 (d, IH), 4.18 (dt, IH), 4.09 (d, IH), 3.73 (dt, IH), 3.37 (dt, IH), 3.15 (td, IH), 2.96 (s, 3H), 2.96 (m, IH), 2.53 (s, 3H), 2.44 (m, IH), 2.35 (m, IH), 1.87 (dddd, IH), 1.69 (m, IH). Chiral HPLC: Rt= 20.8 min.

Example 19: Compound 19

/V--T [3,5-bis(tnfluoromethyn phenyl] methyl - 7-(hydroxymethyl)-/V-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(enantiomer 1 of diaste guration at Cl-C8a)

To a stirred solution of Intermediate 21 (59 mg, 0.1 mmol) in MeOH (3 ml_) was added calcium chloride (17 mg, 0.15 mmol). The resulting suspension was cooled to 0°C and sodium borohydride (12 mg, 0.31 mmol) was added. The reaction mixture was stirred at 25 °C for 2h, then HCI 1M and DCM were added. The aqueous layer was extracted several times with DCM and the combined organic layers were filtered through a phase separator and concentrated in vacuo to give a crude (45 mg) which was subjected to chiral preparative HPLC. Compound 19 (13 mg) was then isolated as single enantiomer. Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2-Propanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 9.4 min. H NMR (500 MHz, CDCI₃) δ ppm 7.75 (s, IH), 7.37 (s, 2H), 7.22 (m, 4H), 4.69 (d, IH), 4.36 (d, IH), 4.17 (dt, IH), 4.10 (d, IH), 3.95 (br. s, IH), 3.73 (m, 2H), 3.40 (dt, IH), 3.17 (td, IH), 3.00 (td, IH), 2.96 (s, 3H), 2.63 (spt, IH), 2.53 (s, 3H), 1.96 (ddd, IH), 1.55 (m, IH). UPLC- MS: Rt=1.15 min; m/z (ES+): 544.28 [M + H] ⁺ . Example 20: Compound 20

A/-- r3,5-bis(trifluoromethyl) phenyl^"! methyl - 7-(hvdroxymethyl)-/V-methyl-l-(2- methyl phenyl) -6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(enantiomer 1 of diastereoisomer 2, single isomer with ANTI configuration at Cl-C8a)

From the same preparation where Compound 19 is described, Compound 20 (3.5 mg) was isolated as single enantiomer. UPLC-MS: Rt= 1.14 min; m/z (ES+): 544.30 [M + H] ⁺ Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2-Propanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 12.4 min. *H NMR (500 MHz, CDCI₃) δ ppm 7.74 (s, IH), 7.36 (s, 2H), 7.18 (m, 3H), 4.69 (d, IH), 4.35 (d, IH), 4.21 (ddd, IH), 4.08 (d, IH), 3.87 (dd, IH), 3.77 (ddd, IH), 3.67 (dd, IH), 3.35 (ddd, IH), 3.21 (td, IH), 2.97 (s, 3H), 2.95 (td, IH), 2.76 (dtd, IH), 2.53 (s, 3H), 1.83 (ddd, IH), 1.72 (ddd, IH).

Example 21: Compound 21

/V--f|^"3,5-bis(trifluoromethyl) phenyl] methyl - 7-(hydroxymethyl)-/V-methyl-l-(2- methy I phenyl) -6-oxo-octahydropyrrolo[l,2-alpiperazine-2-carboxamide diastereomeric mixture of diastereoisomers

(mixture of enantiomer 2 of diastereoisomer 1 plus enantiomer 2 of diastereoisomer 2, single isomer with ANTI configuration at Cl-C8a)

From the same preparation where Compound 19 is described, Compound 21 (17.6 mg) was isolated. UPLC-MS: Rt= 1.13; m/z (ES): 544.33 [M + H] ⁺ ; Rt=1.14; m/z (ES+): 544.30 [M + H] ⁺ . Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2- Propanol 90/10 v/v. Flow rate: 1 mL/min. Detection: DAD at 220 nm. Rt= 16.1 min and 16.8 min.

Example 22: Compound 22 /V--T r3,5-bis(tnfluoromethvn phenyl^"! methyl - 7-(hvdroxymethyl)-/V-methyl-l-(2- methyl phenyl) -6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(single isomer, enantiomer 2 of diastereoisomer 1 in Compound 21)

Separation by chiral chromatography of Compound 21 provided 9.5 mg of Compound 22 (enantiomer 1). ^JH NMR (500 MHz, CDCI₃) δ ppm 7.75 (s, IH), 7.37 (s, 2H), 7.22 (m, 4H), 4.69 (d, IH), 4.36 (d, IH), 4.17 (dt, IH), 4.11 (d, IH), 3.73 (m, 2H), 3.40 (ddd, IH), 3.17 (m, IH), 3.00 (td, 4H), 2.96 (s, 3H), 2.63 (m, IH), 2.53 (s, 3H), 1.96 (ddd, IH), 1.55 (m, IH). Column: Chiralpak AS-H (25 x 0.46 cm), 5μ Mobile phase: n-

Hexane/Ethanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt=10.4 min.

Example 23: Compound 23

(single isomer, enantio 1)

Separation by chiral chromatography of Compound 21 provided 2.5 mg of Compound 23 (enantiomer 2). Column: Chiralpak AS-H (25 x 0.46 cm), 5μ Mobile phase: n- Hexane/Ethanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt=14.7 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.74 (s, IH), 7.36 (s, 2H), 7.18 (m, 3H), 4.69 (d, IH), 4.35 (d, IH), 4.21 (ddd, IH), 4.08 (d, IH), 3.87 (dd, IH), 3.77 (ddd, IH), 3.67 (dd, IH), 3.35 (ddd, IH), 3.21 (td, IH), 2.97 (s, 3H), 2.95 (td, IH), 2.76 (dtd, IH), 2.53 (s, 3H), 1.83 (ddd, IH), 1.72 (ddd, IH). Example 24: Compound 24

N-- r3,5-bis(tnfluoromethyl^')phenyl1methyl -N-methyl-l-(2-methylphenyl^')- octahvdropyrrolori,2-a1piperazine-2-carboxamide

(mixture of enantiomers,

Triphosgene (30 mg, 0.088 mmol) was dissolved in EtOAc (1 ml_). The solution was cooled to 0°C and a solution of Intermediate 23 (48 mg, 0.22 mmol) in EtOAc (2 ml_) and TEA (100 μΙ_) were added. The reaction mixture was stirred for 1.5h, then

Intermediate 3 (80 mg, 0.3 mmol) in EtOAc (2 mL) and TEA (50 μΙ_) were added. The reaction was stirred at 25°C for 2h. To the mixture was added NaOH 1M and the organic layer was dried over sodium sulphate, filtered and concentrated in vacuo. The crude was purified by SPl (SNAP-NH cartridge, 11 g, CH/EtOAc 9:1 to EtOAc as eluent), to give the title compound (50 mg). ^JH NMR (400 MHz, CDCI₃) δ ppm 7.73 (br, 1H), 7.41 (br, 2H), 7.26-7.24 (m, 1H), 7.15-7.07 (m, 3H), 4.63 (d, 1H), 4.46 (d, 1H), 4.27 (d, 1H), 3.42- 3.36 (m, 1H), 3.20-3.12 (m, 3H), 2.93 (s, 3H), 2.52 (s, 3H), 2.51-2.44 (m, 1H), 2.25- 2.10 (m, 2H), 1.88-1.75 (m, 1H), 1.66-1.48 (m, 2H), 1.44-1.34 (m, 1H). UPLC-MS: Rt=0.90 min; m/z (ES+): 500.33 [M + H] ⁺ . Example 25: Compound 25

2-N-rr3,5-bisrtrifluoromethvnphenyllmethyl -2-N,7-N,7-N,7-tetramethyl- 1-Γ2- methylphenyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-2,7-dicarboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

A solution of Compound 8 (13 mg, 0.023 mmol), in DCM (1 mL), was added to a solution of EDCI.HCI (8.62 mg, 0.045 mmol) and HOBT-H₂0 (6.1 mg, 0.045 mmol) in DCM (2 mL). To this stirring mixture was added a solution of (CH₃)₂NH-HCI (3 mg, 0.034 mmol) and TEA (12.7 mL, 0.091 mmol) in 1 mL of DCM. The reaction was left stirring at RT for 2h, then the mixture was diluted with DCM, water was added and the phases were separated. The organic layer was washed with HCI 1M, then an aqueous saturated solution of NaHC0₃ and brine. The organic layer was filtered through a phase separator and the solvent was evaporated. The crude was purified by flash chromatography (SNAP lOg, eluting from CH/EtOAc 9:1 to EtOAc 100%). The fractions were collected and the solvent removed in vacuo to give the title compound (9 mg). UPLC-MS: Column: Acquity UPLC BEH C18 column; m/z (ES+): 599.3 [M + H]⁺ Rt=1.2 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.75 (s, 1H), 7.37 (s, 2H), 7.29 (s, 2H), 7.18 (m, 2H), 4.69 (d, .7=15.4Hz, 1H), 4.38 (d, .7=15.4 Hz, 1H), 4.19 (m, 2H), 3.75 (q, .7=7.8 Hz, 1H), 3.42 (dt, .7=11.7, 2.9 Hz, 1 H), 3.18 (td, .7=12.5, 3.7 Hz, 1H), 3.06 (br s, 6H), 3.00 (m, 4H), 2.53 (s, 3H), 2.13 (dd, .7=12.7, 9.5 Hz, 1H), 1.77 (dd, .7=13.4, 7.1Hz, 1H), 1.39 (s, 3H).

Example 26: Compound 26

2-N-rr3,5-bisrtrifluoromethvnphenyllmethyl -2-N,7-N,7-N,7-tetramethyl- 1-Γ2- methylphenyl)-6-oxo-octahvdropyrrolori,2-a1piperazine-2,7-dicarboxamide

(pure enantiomer, wit

A solution of Compound 8 (12 mg, 0.021 mmol), in DCM (1 mL), was added to a solution of EDCI-HCI (8 mg, 0.042 mmol) and HOBT-H₂0 (5.6 mg, 0.042 mmol) in DCM (2 mL). To this stirring mixture was added a solution of (CH₃)₂NH-HCI (2.6 mg, 0.031 mmol) and TEA (11.7 mL, 0.083 mmol) in 1 mL of DCM. The reaction was left stirring at RT for 2h, then the mixture was diluted with DCM, water was added and the phases were separated. The organic layer was washed with HCI 1M, then an aqueous saturated solution of NaHC0₃ and brine. The organic layer was filtered through a phase separator and the solvent was evaporated. The crude was purified by flash chromatography (SNAP lOg, eluting from CH/EtOAc 9:1 to EtOAc 100% to DCM/EtOAc 9:1). The fractions were collected and the solvent removed in vacuo to give the title compound (9 mg). UPLC- MS: Column: Acquity UPLC BEH C18 column; m/z (ES+): 599.3 [M + H]⁺ Rt=1.19 min. ^JH NMR (500 MHz, CDCI₃)) δ ppm 7.75 (s, IH), 7.37 (s, 2H), 7.28 (m, 2H), 7.18 (m, 2H), 4.69 (d, 3= 15 A Hz, IH), 4.37 (d, .7= 14.9 Hz, IH), 4.19 (m, 2H), 3.75 (q, 7=7.8 Hz, IH), 3.42 (dt, 7= 11.0, 0.5 Hz, IH), 3.18 (td, 7= 11.5, 2.9 Hz, IH), 3.06 (br s, 6H), 3.00 (m, 4H), 2.52 (s, 3H), 2.13 (dd, 7= 12.7, 8.8 Hz, IH), 1.77 (dd, 7= 13.2, 6.8 Hz, IH), 1.39 (s, 3H).

Example 27: Compound 27

N-- r3,5-bis(tnfluoromethyl^')phenyl1methyl -7-(hvdroxymethyl^')-N-methyl-l-(2- methylphenvD- octahvdropyrrolor i,2-a1piperazine-2-carboxamide; methanesulfonic acid salt

_(enantiomer 1, single enantiomer with ANTI configuration at Cl-C8a)

Intermediate 26 (270 mg, 0.5 mmol), was dissolved in dry THF (20 mL) at 0°C,

BH₃.Me₂S (2M in THF) ( 1 mL), was added dropwise. The reaction mixture was stirred at RT for 16 h. BH₃. Me₂S (2 M in THF) (1 mL) was added again and the reaction was left stirring at RT for a further 8h. HCI (1M) (2 mL) and MeOH (2 mL) were then added and the reaction mixture was stirred overnight. The reaction mixture was concentrated in vacuo, DCM (20 mL) was added followed by a aqueous saturated solution of NaHC0₃ (30 mL). The organic layer was dried over sodium sulphate, filtered and evaporated in vacuo to give a colourless oil (210 mg) which was subjected to chiral prep. HPLC. Column Chiralpak AD-H (25 x 0.46 cm), 5 urn; Mobile phase: n-Hexane/2-Propanol 90/10 % v/v; Flow rate (ml/min) : 1.0; DAD detection : 220 nm; Loop: 20 μί; enantiomer 1 : 50 % a/a by UV (5.9 min); enantiomer 2: 50 % a/a by UV (12.2 min). Thus, two fractions were recovered (fraction 1 containing the first eluting enantiomer, enantiomer 1, 95 mg) and fraction 2 (containing the second eluting enantiomer: enantiomer 2, 105 mg, described below). Fraction 1 (95 mg, 0.18 mmol) was dissolved in THF (3 mL) and a solution of methanesulfonic acid (11.7 mL, 0.18 mmol) in dry THF (1 mL) was added at 0°C and the reaction mixture was stirred 30' at this temperature. The solvents were evaporated in vacuo to give 102 mg of a white solid. UPLC/MS (ES+/ES-) 2.0 Minute; Method : LC/MS System : Acquity UPLC coupled with SQD mass spectrometer: LC/MS Conditions: Column: Acquity UPLC BEH C18 column. MS Conditions: Ionisation mode: alternate Positive/Negative Electrospray (ES+/ES-); Rt=1.22 min a/a. m/z (ES+): 530 [M + H] ⁺ . ^JH NMR (500 MHz, CDCI₃) δ ppm 10.59 (br. s, 1H), 7.67 (s, 1H), 7.27 (s, 2H), 7.09 (m, 4H), 4.70 (m, J=10.3 Hz, 2H), 4.14 (m, 7=14.2 Hz, 2H), 4.02 (d, 7=11.2 Hz, 1H), 3.61 (m, 3H), 3.46 (d, 7=13.7 Hz, 1H), 3.23 (m, 1H), 2.99 (m, 2H), 2.87 (s, 3H), 2.81 (s, 3H), 2.49 (m, 1H), 2.46 (s, 3H), 1.75 (m, 7=8.3, 2.9 Hz, 2H).

Example 28: Compound 28

N-- r3,5-bis(tnfluoromethyl^')phenyl1methyl -7-(hvdroxymethyl^')-N-methyl-l-(2- methyl phenyl)-octahvdropyrrolori,2-a1 pi perazine-2-carboxamide; methanesulfonic acid salt

(enantiomer 2, single enantiomer with ANTI configuration at Cl-C8a)

Fraction 2 (from the above described experimental), (105 mg, 0.2 mmol) containing the second eluting enantiomer, enantiomer 2, was dissolved in THF (3 ml_) and a solution of methanesulfonic acid (13 ml_, 0.18 mmol) in dry THF (1 ml_) was added at 0°C and the reaction mixture was stirred 30' at this temperature. The solvents were evaporated in vacuo to give 98 mg of a white solid. *H NMR (500 MHz, CHLOROFORM-d) δ ppm 10.66 (br. s, 1H), 7.74 (s, 1H), 7.34 (s, 2H), 7.17 (m, 4H), 4.77 (m, J = 10.3 Hz, 2H), 4.22 (m, J = 14.2 Hz, 2H), 4.10 (d, 2 = 11.2 Hz, 1H), 3.69 (m, 3H), 3.54 (d, 2 = 13.7 Hz, 1H), 3.31 (m, 1H), 3.07 (m, 2H), 2.94 (s, 3H), 2.89 (s, 3H), 2.57 (m, 1H), 2.54 (s, 3H),1.83 (m, J = 8.3, 2.9 Hz, 2H) UPLC/MS Electrospray (ES+/ES-); Rt=1.22 min a/a. (ES+): 530.2 [M + H] ⁺ .

Example 29: Compound 29

Ν--Γ [3, 5-bis(trifluoromethyl) phenyl] methyl -N-methyl- l-(2-methyl phenyl)-7-(morpholi n-

4-ylmethyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-2-ca rboxamide

(mixture of enantiomer 2 of diastereoisomer 1 plus enantiomer 2 of diastereoisomer 2, single stereoisomer with ANTI configuration at Cl-C8a)

A solution of Intermediate 33 (68 mg, 0.109 mmol) and morpholine (96 μΙ_, 1.09 mmol) in dry THF (1.5 mL) was heated at 65°C under stirring for 48h. The solvent was removed in vacuo and the residue was dissolved in EtOAc (10 mL) and washed with saturated NaHC0₃ (3x5mL). The organic layer was dried over Na₂S0₄, filtered and concentrated in vacuo. The residue was dissolved in 1 mL of meOH and filtered throught a SCX cartridge (Strata-SCX, 100 mg, Phenomenex, eluting with ammonia 2M solution in MeOH).

Concentration of opportune fractions provided 29 mg of a crude which was purified by preparative HPLC.LC/MS System: Fractionlynx (Waters) with ZQ MS detector. UV Conditions: UV detection range: 210 nm to 350 nm; Acquisition rate: 1.0 spectra/s; MS Conditions: Ionisation mode: Positive Electrospray (ES+); Scan Range: ES+ 100 to 900 AMU: Scan Duration: 0.50 seconds; Columns: XBridge Prep. C185 μιη OBD (100mm x 19.0; mm) at RT; 9 mg of the title compound were recovered as a 75:25 mixture of diastereoisomers. *H NMR (400 MHz, CDCI₃) δ ppm 7.74 (br s), 7.37 (br s), 7.27-7.10 (m), 4.68 (d), 4.40-4.33 (m), 4.22-4.15 (m), 4.06 (d), 3.80-3.60 (m), 3.40-3.30 (m), 3.20-3.10 (m), 3.00-2.90 (m), 2.88-2.80 (m), 2.75-2.30 (m), 2.05-1.95 (m), 1.92-1.75 (m), 1.70-1.60 (m) UPLC-MS: Rt=1.22; m/z (ES+): 613 [M + H] ⁺ ; Rt=1.23; m/z (ES+): 613 [M + H] ⁺ ; Rt=1.24 min; m/z (ES+): 613 [M + H] ⁺ . Example 30: Compound 30

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)-6-oxo-7- (pyrrolidin-l-ylmethyl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(diastereoisomer 1, ANTI stereochemistry at Cl-C8a, ANTI stereochemistry at C1-C7)

A solution of Intermediate 33 (97 mg, 0.156 mmolO and pyrrolidine (130 μΙ_, 1.56 mmol) in dry THF (2 ml_) was heated at 65°C under stirring for 20h. Solvent was removed in vacuo and the residue was dissolved in EtOAc and washed with saturated NaHC0₃ solution (3x5ml_). the organic layer was dried over Na₂S0₄, filtered and concentrated in vacuo. The residue was dissolved in 1 ml_ of MeOH and filtered through a SCX

(Phenomenex, 2000 mg). Elution with only MeOH provided a first fraction which was subjected to preparative HPLC: Column: X-Bridge Prep C-18 (19 x 100 mm), 5 μ; Mobile phase Amm Bicarbonate, pH = 10/Acn 65/35 % v/v -> 25/75 in lOmin; Flow rate

(ml/min) 17 mL/min; DAD detection 220 nm; Loop 1000 μί; Total amount 40 mg;

Solubilization 40 mg/mL in 3 mL Acn = 13.3 mg/mL; Rt= 9.36 min to provide a crude which was further purified as follows: elution with solution of ammonia 2M in MeOH, gave a fraction which was further purified by preparative HPLC. Column: BEH C-18 (2.1 x 50 mm), 1.7 urn; Mobile phase: Amm. Bicarbonate, pH = 10/Acn 97/3 % v/v -> 0/100 in 1.5 min; Flow rate (mL/min): 1.0; DAD detection: 210-350 nm; Loop: 20 μί;

diastereoisomer 1, 21.8% ee (1.33 min); diastereoisomer 2, 41 % ee (1.38 min). After evaporation of the two fractions obtained, two products were obtained: isomer 1

(Compound 30) and isomer 2 (Compound 31, described below). Compound 30 (16 mg): ^JH NMR (400 MHz, CDCI₃) δ ppm 7.66 (s, IH), 7.29 (s, 2H), 7.07 (m, 3H), 4.60 (d,

.7=15.3 Hz, IH), 4.29 (d, 7=15.3 Hz, IH), 4.08 (dt, 7=12.9, 2.7 Hz, IH), 3.99 (d, 7=9.8 Hz, IH), 3.58 (dt, 7=9.8, 7.8 Hz, IH), 3.30 (dt, 7=11.7, 2.7 Hz, IH), 3.07 (td, 7=12.3, 3.1 Hz, IH), 2.89 (m, 5H), 2.48 (m, 9H), 1.99 (dt, 7=13.1, 7.7 Hz, IH), 1.62 (m, 5 H). UPLC-MS: Rt=1.31 min; m/z (ES+): 597.3 [M + H] ⁺

Example 31: Compound 31

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)-6-oxo-7-

(pyrrolidin-l-ylmethyl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(diastereoisome 2, ANT mistry at C1-C7)

After evaporation of fraction collected by preparative HPLC from the above described experimental, Compound 31 was obtained (5 mg). ¹ NMR (400 MHz, CDCI₃) δ ppm 7.74 (s, IH), 7.37 (s, 2H), 7.15 (m, 3H), 4.67 (d, 7=15.7 Hz, IH), 4.36 (d, 7=15.7 Hz, IH), 4.20 (dt, .7=12.9, 2.7 Hz, IH), 4.06 (d, J=10.2 Hz, IH), 3.74 (ddd, 7=9.4, 8.2, 5.9 Hz, IH), 3.33 (dt, 7=12.1, 2.3 Hz, IH), 3.15 (td, 7=12.9, 3.5 Hz, IH), 2.95 (m, 4H), 2.73 (m, 2H), 2.52 (m, 8H), 1.87 (m, 2H), 1.74 (m, 4H). UPLC-MS: Rt=1.33 min; m/z (ES+): 597.3 [M + H] ⁺ .

Example 32: Compound 32

N-- r3,5-bis(tnfluoromethvnphenyl1methyl -N-methyl-7-methylidene-l-(2- methylphenvn-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

After evaporation of fraction collected by preparative HPLC, Compound 32 was obtained (5 mg). ^JH NMR (400 MHz, CDCI₃) δ ppm 7.66 (s, IH), 7.29 (s, 2H), 7.10 (m, 3H), 5.96 (t, IH), 5.26 (t, IH), 4.62 (d, IH), 4.27 (d, IH), 4.23 (dt, IH), 3.97 (d, IH), 3.71 (m, IH), 3.31 (m, IH), 3.17 (td, IH), 2.92 (td, IH), 2.89 (s, 3H), 2.51 (m, IH), 2.44 (s, 3 H), 2.29 (m, IH). UPLC-MS: Rt=1.28 min; m/z (ES+): 526.2 [M + H] ⁺

Example 33: Compound 33

N-- i-r3,5-bis(trifluoromethyl^')phenyl1-3-hvdroxypropyl -7-(2-hvdroxyethyl^')-N-methyl- l-(2-methylphenvn-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(mixture of stereoisomers with ANTI configuration at Cl-C8a and SYN configuration at C1-C7)

NaBH₄ (10 mg, 0.268 mmol) was added to an ice cooled solution of Intermediate 32 (80 mg, 0.134 mmol) in MeOH (5 mL), the resulting solution was stirred for 30 min. MeOH was evaporated in vacuo, the residue was dissolved with DCM and washed with NH₄CI ss. The organic phase was filtered through a phase separator and the solvent was evaporated. The crude was purified by flash chromatography (SNAP lOg, eluting from DCM 100% to DCM/MeOH 85:15). The fractions were collected and the solvent removed in vacuo to give the title compound as white solid (50 mg). *H NMR (400 MHz, CDCI₃) δ ppm 7.68 (s, IH), 7.29 (s, 2H), 7.12 (m, 5H), 5.57 (dd, 7=11.3, 3.5 Hz, IH), 4.13 (ddd, 7=13.3, 3.1, 2.0 Hz, IH), 3.98 (d, 7=10.2 Hz, IH), 3.70 (m, 4H), 3.38 (m, IH), 3.43 (dd, 7=6.7, 4.7 Hz, IH), 3.22 (ddd, 7=12.1, 3.5, 1.6 Hz, IH), 3.10 (td, 7=12.5, 3.9 Hz, IH), 2.85 (td, 7=12.1, 3.1 Hz, IH), 2.69 (s, 3H), 2.64 (m, IH), 2.43 (s, 3H), 2.08 (m, IH), 1.95 (m, IH), 1.80 (m, 2H), 1.59 (m, 2H) UPLC-MS: Rt=1.07 min; m/z (ES+): 602.3 [M + H] ⁺ .

Example 34: Compound 34

Ν--Γ1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl -7-(2-hydroxyethyl)-N-methyl- l-(2-methylphenyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(enantiomeric pair with ANTI confi uration at Cl-C8a and syn configuration at C1-C7)

Separation by chiral chromatography of 22 mg of Compound 33 provided 5.3 mg of Compound 34 Column: Chiralcel OD-H (25 x 0.46 cm), 5μ Mobile phase: n-

Hexane/Ethanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 25.1 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.68 (s, IH), 7.29 (s, 2H), 7.12 (m, 5H), 5.57 (dd, 7=11.3, 3.5 Hz, IH), 4.13 (ddd, 7=13.3, 3.1, 2.0 Hz, IH), 3.98 (d, 7=10.2 Hz, IH), 3.70 (m, 4H), 3.38 (m, IH), 3.43 (dd, 7=6.7, 4.7 Hz, IH), 3.22 (ddd, 7=12.1, 3.5, 1.6 Hz, IH), 3.10 (td, 7=12.5, 3.9 Hz, IH), 2.85 (td, 7=12.1, 3.1 Hz, IH), 2.69 (s, 3H), 2.64 (m, IH), 2.43 (s, 3H), 2.08 (m, IH), 1.95 (m, IH), 1.80 (m, 2H), 1.59 (m, 2H).

Example 35: Compound 35

(enantiomeric pair with ANTI configuration at Cl-C8a and syn configuration at C1-C7)

Separation by chiral chromatography of 22 mg of Compound 33 provided 7.2 mg of Compound 35. Column: Chiralcel OD-H (25 x 0.46 cm), 5μ Mobile phase: n- Hexane/Ethanol 90/10 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 32.8 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.68 (s, IH), 7.29 (s, 2H), 7.12 (m, 5H), 5.57 (dd, 7=11.3, 3.5 Hz, IH), 4.13 (ddd, 7=13.3, 3.1, 2.0 Hz, IH), 3.98 (d, 7=10.2 Hz, IH), 3.70 (m, 4H), 3.38 (m, IH), 3.43 (dd, 7=6.7, 4.7 Hz, IH), 3.22 (ddd, 7=12.1, 3.5, 1.6 Hz, IH), 3.10 (td, 7=12.5, 3.9 Hz, IH), 2.85 (td, 7=12.1, 3.1 Hz, 1 H), 2.69 (s, 3 H), 2.64 (m, 1 H), 2.43 (s, 3 H), 2.08 (m, 1 H), 1.95 (m, 1 H), 1.80 (m, 2 H), 1.59 (m, 2 H).

Example 36: Compound 36

Ν--Γ1 -[3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl -7-(2-hydroxyethy l)-N-methyl- l-(2-methylphenyl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

To a 0°C cooled solution of Compound 33 (30 mg, 0.05 mmol) in THF (3 mL), a solution of borane dimethylsulfide complex 2M in THF (0.100 mL, 0.2 mmol) was added dropwise. The reaction mixture was stirred overnight at 25°C. MeOH (1 mL) and HCI IN (lml) were carefully added and the reaction mixture was stirred at 25°C for 2h. HCI 1M was added and the mixture was stirred 6h. The solution was evaporated and the crude material was charged the residue was filtered through an SCX cartridge eluting with NH₃ in MeOH 2M solution. The solvent was removed in vacuo to give the title compound as white solid (15 mg). ^JH NMR (400 MHz, CD₃OD) δ ppm 7.78 (s, IH), 7.55 (s, 2H), 7.23 (d, 7=7.0 Hz, IH), 7.05 (m, 3H), 5.50 (t, 7=7.4 Hz, IH), 4.30 (d, 7=9.8 Hz, IH), 3.53 (m, 6H), 3.08 (t, 7=12.5 Hz, IH), 2.90 (s, 3H), 2.74 (m, IH), 2.59 (m, IH), 2.48 (s, 3H), 2.34 (m, IH), 2.17 (m, 3H), 1.81 (q, 7=11.0 Hz, IH), 1.50 (quin, 7=6.7 Hz, 2H), 1.09 (m, IH). HPLC-MS: Rt=1.14 min; m/z (ES+): 588.3 [M + H] ⁺ .

Example 37: Compound 37

7- r(4-acetylpiperazin-l-yl^')methyl1-N-- r3,5-bis(tnfluoromethyl^')phenyl1 methyl -N- methyl-l-(2-methylphenvn-6-oxo-octahvdropyrrolori,2-a1piperazine-2-ca rboxamide (diastereoisomeic mixture with ANTI configuration at Cl-C8a)

A solution of Intermediate 33 (34 mg, 0.055 mmol) and N-acetylpiperazine (70 mg, 0.55 mmol) in THF (3 ml_) was heated at reflux for 72h. The solvent was removed in vacuo and the residue was purified by HPLC preparative column in acid conditions to obtain the title compound as a pale yellow solid (9 mg): H NMR (400 MHz, CDCI₃) δ ppm 7.67 (s, IH), 7.29 (s, 2H), 7.09 (m, 3H), 4.61 (d, 7=15.7 Hz, IH), 4.28 (d, 7=14.1 Hz, IH), 4.08 (dt, 7=13.3, 2.7 Hz, IH), 3.98 (d, 7=10.2 Hz, IH), 3.63 (m, 2H), 3.37 (m, 4H), 3.08 (td, 7=12.3, 3.1 Hz, IH), 2.88 (s, 3H), 2.84 (m, 2H), 2.48 (s, 3H), 2.50 (m, 2H), 2.32 (m, 4H), 2.00 (s, 3H), 1.97 (m, IH). HPLC-MS: Rt=1.14 min; m/z (ES+): 654 [M + H] ⁺ .

Example 38: Compound 38

Ν--Γ [3, 4-bis(trifluoromethyl) phenyl] methyl -N-methyl- l-(2-methyl phenyl)-7-(morpholi n- 4-ylmethyl)-6-oxa-octahyd ropy rrolo[l,2-al pi perazine-2-ca rboxamide methansulfonic acid salt

(enantiomer 1 of diastereoisomer 1, single isomer with ANTI configuration at Cl-C8a)

Compound 29 was subjected to chiral prep. HPLC and four fractions were recovered: Compound 38, described here, and Compound 39, 40 and 41, described below.

Compound 38: column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2- Propanol 88/12 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 10.6 min. The sample recovered (150 mg, 0.245 mmol) was dissolved in THF (3 ml) and the solution was cooled at 0°C, then a solution of methansulfonic acid (16 μΙ_, 0.245 mmol) in THF (1 ml_) was added dropwise. The resulting solution was stirred for 30 min then the solvent was evaporated, the solid was triturated with Et₂0 and dried overnight in the vacuum pump at 50°C to obtain the title compound as pale yellow-white solid (163 mg) ¹ NMR (500 MHz, DMSO-d₆) δ ppm 9.41 (br s, 1H), 7.96 (s, 1H), 7.60 (s, 2H), 7.34 (m, 1H), 7.11 (m, 3H), 4.58 (d, .7=15.7 Hz, 1 H), 4.48 (d, .7=15.7 Hz, 1H), 4.02 (d, .7=10.3 Hz, 1H), 3.94 (br. d, .7=12.2 Hz, 2H), 3.86 (dt, .7=13.2, 2.9 Hz, 1H), 3.70 (td, .7=9.4, 6.6 Hz, 1H), 3.55 (m, 5H), 3.37 (m, 1H), 3.23 (m, 2H), 3.13 (m, 1H), 3.02 (m, 1H), 2.88 (s, 3H), 2.87 (m, 2H), 2.47 (s, 3H), 2.30 (s, 3H), 2.03 (ddd, .7=12.2, 7.8, 6.4 Hz, 1H), 1.52 (q, .7=10.7 Hz, 1H). HPLC-MS: Rt=1.23 min; m/z (ES+): 613 [M + H] ⁺ .

Example 39: Compound 39

N--[3,4-bis(trifluoromethyl)phenyllmethyl -N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahydropyrrolo[l,2-alpiperazine-2-carboxamide as methansulfonic salt

(enantiomer 2 of diastereoisomer 1, single isomer with ANTI configuration at Cl-C8a)

From the above described chiral prep. Choromatography on Compound 29, Compound 39 was also obtained. Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n- Hexane/2-Propanol 88/12 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 18.9. The sample recovered (150 mg, 0.245 mmol) was dissolved in THF (3 ml_) and the solution was cooled at 0°C, then a solution of methansulfonic acid (16 μΙ_, 0.245 mmol) in THF (ImL) was added dropwise. The resulting solution was stirred for 30 min then the solvent was evaporated, the solid was triturated with Et₂0 and dried overnight in the vacuum pump at 50°C to obtain the title compound as pale yellow-white solid (156 mg) ^JH NMR (500 MHz, DMSO-d₆) δ ppm 9.41 (br s, 1H), 7.96 (s, 1H), 7.59 (s, 2H), 7.34 (m, 1H), 7.10 (m, 3H), 4.58 (d, .7=15.7 Hz, 1H), 4.48 (d, .7=15.7 Hz, 1H), 4.02 (d, .7=9.8 Hz, 1H), 3.94 (d, .7=12.7 Hz, 2H), 3.86 (dt, .7=12.7, 2.5 Hz, 1H), 3.70 (m, 1H), 3.55 (m, 5H), 3.36 (m, 1H), 3.23 (m, 2H), 3.15 (m, 1H), 3.03 (m, 1H), 2.88 (s, 3H), 2.84 (m, 2H), 2.47 (s, 3H), 2.29 (s, 3H), 2.03 (m, 1H), 1.52 (m, 1H). HPLC-MS: Rt=1.23; m/z (ES+): 613 [M + H] ⁺ .

Example 40: Compound 40

N-- [3,4-bis(trifluoromethyl)phenyllmethyl -N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahydropyrrolo[l,2-alpiperazine-2-carboxamide as methansulfonic salt

From the above described chiral prep. Chromatography on Compound 29, Compound 40 was also obtained. Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n- Hexane/2-Propanol 88/12 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 13.8 min. The sample recovered (62 mg, 0.101 mmol) was dissolved in THF (3 ml) and the solution was cooled at 0°C, then a solution of methansulfonic acid (6.5 μί, 0.101 mmol) in THF (ImL) was added dropwise. The resulting solution was stirred for 30 min then the solvent was evaporated, the solid was triturated with Et₂0 and dried overnight in the vacuum pump at 50°C to obtain the title compound as pale yellow-white solid (73 mg) ^JH NMR (500 MHz, DMSO-d₆) δ ppm 9.31 (br s, 1H), 7.96 (s, 1H), 7.59 (s, 2H), 7.34 (m, 1H), 7.11 (m, 3H), 4.57 (d, .7=15.7 Hz, 1H), 4.47 (d, .7=15.7 Hz, 1H), 4.04 (d, .7=10.3 Hz, 1H), 3.94 (m, 3H), 3.80 (td, .7=9.2, 4.6 Hz, 1H), 3.63 (m, 2H), 3.47 (m, 2H), 3.38 (m, 2H), 3.25 (m, 1H), 3.17 (m, 3H), 3.04 (m, .7=12.2 Hz, 1H), 2.89 (s, 3H), 2.76 (td, .7=11.7, 2.9 Hz, 1H), 2.45 (s, 3H), 2.30 (s, 3H), 1.82 (ddd, .7=13.6, 9.2, 4.6 Hz, 1H), 1.72 (m, 1H). HPLC-MS: Rt=1.24 min; m/z (ES+): 613 [M + H] ⁺ .

Example 41: Compound 41

N-- r3,4-bis(tnfluoromethyl^')phenyl1methyl -N-methyl-l-(2-methylphenyl^')-7-(morpholin- 4-ylmethyl)-6-oxa-octahvdropyrrolori,2-a1piperazine-2-carboxamide as methansulfonic salt

(enantiomer 2 of diaste uration at Cl-C8a)

From the above described chiral prep. Choromatography on Compound 29, Compound 39 was also obtained. Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n- Hexane/2-Propanol 88/12 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 15.4 min. The sample recovered (62 mg, 0.101 mmol) was dissolved in THF (3 ml) and the solution was cooled at 0°C, then a solution of methansulfonic acid (6.5 μΙ_, 0.101 mmol) in THF (lmL) was added dropwise. The resulting solution was stirred for 30' then the solvent was evaporated, the solid was triturated with Et₂0 and dried overnight in the vacuum pump at 50°C to obtain the title compound as pale yellow-white solid (67 mg) ^JH NMR (500 MHz, DMSO-d₆) δ ppm 9.30 (br s, 1H), 7.96 (s, 1H), 7.59 (s, 2H), 7.34 (m, 1H), 7.11 (m, 3H), 4.57 (d, .7=15.7 Hz, 1H), 4.47 (d, .7=15.7 Hz, 1H), 4.04 (d, .7=10.3 Hz, 1H), 3.95 (m, 3H), 3.80 (td, .7=9.0, 4.9 Hz, 2H), 3.63 (m, 2H), 3.46 (m, 2H), 3.37 (m, .7=10.8 Hz, 2H), 3.25 (m, 1H), 3.15 (m, 3H), 3.04 (m, 1H), 2.89 (s, 3H), 2.76 (td, .7=11.6, 3.2 Hz, 1H), 2.46 (s, 3H), 2.29 (s, 3H), 1.82 (ddd, .7=13.6, 9.2, 4.6 Hz, 1H), 1.72 (m, 1H). HPLC-MS: Rt=1.24 min; m/z (ES+): 613 [M + H] ⁺ . Example 42: Compound 42

N-- [3,5-bis(trifluoromethyl)phenyllmethyl -7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(racemic mixture, ANTI configuration at Cl-C8a)

Intermediate 37 (43 mg) was dissolved in MeOH (5 ml_) and NaBH₄ (10 mg) was added at 0°C. The reaction was left stirring at this temperature for 30min, then the solvent was removed in vacuo and the residue was taken up with HCI IN and DCM. The organic layer was filtered through a phase separator and concentrated in vacuo. The crude was purified by flash chromatography (10 g SNAP cartridge, eluting from Cy/EtOAc 8 : 2 to 0 : 1 and DCM/MeOH 9 : 1). The fractions were collected and the solvent removed to give 35 mg of title compound. UPLC/MS : m/z (ES+) : 601.92 [M + H]⁺ Rt= 1.05min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, 1H), 7.36 (s, 2H), 7.16 (m, 3H), 4.67 (d, J = 15.3 Hz, 1H), 4.34 (d, J = 15.3 Hz, 1H), 4.14 (d, J = 13.3Hz, 1H), 4.07 (d, J =9.8 Hz, 1H), 3.72 (m, 5H), 3.38 (d, J = 12.1 Hz, 1H), 3.15 (td, J = 12.7, 4.1 Hz, 1H), 2.95 (s, 3H), 2.98 (td, J = 12.1, 2.7 Hz, 1H), 2.91(m, 1H), 2.52 (s, 3H), 2.04 (m, 1H), 1.81 (m, 6H).

Example 43 : Compound 43

N-rr3,5-bis(trifluoromethyl)phenyl1methyl -7,7-bis(2-hvdroxyethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(enantiomer 1, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

35 mg of Compound 42 were purified by chiral preparative HPLC obtaining two fractions After evaporation two products were obtained : enantiomer 1 (Compound 43, described here) and enantiomer 2 (Compound 44, described below). Compound 43 : white foam, 12.3 mg. Chiral HPLC, Chiralpak AD-H column (25 x 0.46 cm), 5 μιη, Mobile phase: n- Hexane/2-Propanol 85/15 v/v, Flow rate: 1 mL/min; Detection : DAD at 220 nm. Rt=6.5 min ^JH NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, IH), 7.36 (s, 2H), 7.16 (m, 3H), 4.67 (d, J = 15.3 Hz, IH), 4.34 (d, J = 15.3 Hz, IH), 4.14 (d, J = 13.3Hz, IH), 4.07 (d, J=9.8 Hz, IH), 3.72 (m, 5H), 3.38 (d, J = 12.1 Hz, IH), 3.15 (td, J = 12.7, 4.1 Hz, IH), 2.95 (s, 3H), 2.98 (td, J = 12.1, 2.7 Hz, IH), 2.91(m, IH), 2.52 (s, 3H), 2.04 (m, IH), 1.81 (m, 6H).

Example 44: Compound 44

N-- r3,5-bis(tnfluoromethyl^')phenyl1methyl -7,7-bis(2-hvdroxyethyl^')-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(enantiomer 2, ANTI stereochemistr at Cl-C8a, single unknown stereoisomer)

After evaporation of collected fraction from chiral preparative HPLC from the above described experimental, Compound 44 was obtained (white foam, 11.3 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη. Mobile phase: n-Hexane/2-Propanol 85/15 v/v, Flow rate: 1 mL/min. Detection : DAD at 220 nm. Rt= 11.4 min. *H NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, IH), 7.36 (s, 2H), 7.16 (m, 3H), 4.67 (d, J = 15.3 Hz, IH), 4.34 (d, J = 15.3 Hz, IH), 4.14 (d, J = 13.3Hz, IH), 4.07 (d, J=9.8 Hz, IH), 3.72 (m, 5H), 3.38 (d, J = 12.1 Hz, IH), 3.15 (td, J = 12.7, 4.1 Hz, IH), 2.95 (s, 3H), 2.98 (td, J = 12.1, 2.7 Hz, IH), 2.91(m, IH), 2.52 (s, 3H), 2.04 (m, IH), 1.81 (m, 6H). [M + H]+ CALC: 602.2454; OBSERVED : 602.2450.

Example 45 : Compound 45

Ν--Γ r3,5-bis(trifluoromethyl)phenyl1methyl -N,l-dimethyl-4'-(2-methyl phenyl)- 1 '-oxo- hexahvdro-l'H-spirorpiperidine-4,2'-pyrrolor i ,2-a1piperazine1-5'-carboxamide (racemic mixture with ANTI configuration at Cl-C8a)

Intermediate 37 (16 mg, 0.027 mmol) was dissolved in MeOH (1 ml_). MeNH₂-HCI (1.8 mg, 0.027 mmol) and AcOH (1 drop) were added to the solution and the reaction was left stirring at RT for 10 min, then NaBH₃(CN) was added and the reaction was left stirring at RT overnight. The solution was filtered through a SCX cartridge, eluting with NH₃2M solution in MeOH. The solvent was removed in vacuo, obtaining 11.6 mg of a residue which was dissolved in DCM and washed with NaOH 1M. The organic phase was filtered through a phase separator and concentrated, obtaining 7.8 mg of the title compound. UPLC-MS, m/z (ES+): 596.98 [M + H]⁺ Rt=0.94 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, 1H), 7.36 (s, 2H), 7.20 (m, 3H), 4.68 (d, J = 15.7 Hz, 1H), 4.34 (d, J = 15.7 Hz, 1H), 4.17 (dt, J = 13.7, 2.7 Hz, 1H), 4.02 (d, J=9.8 Hz, 1H), 3.67 (dt, j=9.4, 7.4 Hz, 1H), 3.36 (dt, J = 11.7, 2.7 Hz, 1H), 3.14 (td, J = 11.7, 3.1 Hz, 1H), 2.95 (td, J = 11.7, 3.5 Hz, 1H), 2.95 (s, 3H), 2.83 (m, 1H), 2.69 (m, 1H), 2.52 (s, 3H), 2.24 (s, 3H), 2.20 (m, 1H), 1.91 (m, 4H), 1.46 (m, 2H), 1.33 (m, 1H).

Example 46: Compound 46

Ν--Γ [3, 5-bis(trifluoromethyl) phenyl] methyl -N,l-di methyl-4'-(2-methyl phenyl)- hexahydro-l'H-spiro[piperidine-4,2'-pyrrolo[l,2-alpiperazinel-5'-carboxamide

(enantiomer 1, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

Compound 45 was separated in the corresponding isomers by chiral chromatography, two fractions were obtained, Compound 46 (described here) and Compound 47

(described below). After evaporation of collected fractions from chiral preparative HPLC, Compound 46 was obtained (isomer 1, 68 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/(Ethanol+0.1% isopropylamine) 90/10%v/v, Flow rate: 0.8 mL/min. Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt=9.0 min. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, IH), 7.36 (s, 2H), 7.20 (m, 3H), 4.68 (d, J = 15.7 Hz, IH), 4.34 (d, J = 15.7 Hz, IH), 4.17 (dt,J = 13.7, 2.7 Hz, IH), 4.02 (d, J=9.8 Hz, IH), 3.67 (dt, J=9.4, 7.4 Hz, IH), 3.36 (dt, J = 11.7, 2.7 Hz, IH), 3.14 (td, J = 11.7, 3.1 Hz, IH), 2.95 (td, J = 11.7,3.5 Hz, IH), 2.95 (s, 3H), 2.83 (m, IH), 2.69 (m, IH), 2.52 (s, 3H), 2.24 (s, 3H), 2.20 (m, IH), 1.91 (m, 4H), 1.46 (m, 2H), 1.33 (m, IH).

Example 47: Compound 47

N- r3,5-bis(trifluoromethvnphenyl1methyl -N,l-dimethyl-4'-(2-methylphenvn-l'-oxo- hexahydro-l'H-spiro[piperidine-4,2'-pyrrolo[ l ,2-alpiperazinel-5'-carboxamide

(enantiomer 2, ANTI stereochemistry at Cl-C8a, single unknown stereoisomer)

After evaporation of the second collected fraction from chiral preparative HPLC of the above described experimental, Compound 47 was obtained (isomer 2, 73mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/(Ethanol+0.1% isopropylamine) 90/10%v/v , Flow rate: 0.8 mL/min. Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt= 12.5 min. H NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, IH), 7.36 (s, 2H), 7.20 (m, 3H), 4.68 (d, J = 15.7 Hz, IH), 4.34 (d, J = 15.7 Hz, IH), 4.17 (dt,J = 13.7, 2.7 Hz, IH), 4.02 (d, J=9.8 Hz, IH), 3.67 (dt, J=9.4, 7.4 Hz, IH), 3.36 (dt, J = 11.7, 2.7 Hz, IH), 3.14 (td, J = 11.7, 3.1 Hz, IH), 2.95 (td, J = 11.7,3.5 Hz, IH), 2.95 (s, 3H), 2.83 (m, IH), 2.69 (m, IH), 2.52 (s, 3H), 2.24 (s, 3H), 2.20 (m, IH), 1.91 (m, 4H), 1.46 (m, 2H), 1.33 (m, IH).

Example 48: Compound 48

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -7-(hvdroxymethyl)-N-methyl-l-(2- methylphenyl)-octahvdropyrrolor i,2-a1piperazine-2-carboxamide

(enantiomeric pair, ANTI at C2-C8a, diastereoisomer 1)

Separation by HPLC chromatography of Intermediate 38 provided two fractions,

Compound 48, described here, and Compound 49, described below. Compound 48: 4.5 mg, isomer 1: column: X Bridge C-18 BOD (19 x 100 mm), 5μ Mobile phase: Ammonium Bicarbonate, pH + 10, 10 mM/ACN 80/20% v/v>25/75 in 10 min> 0/100 in 1 min. Flow rate 17 mL/min Detection: DAD at 225 nm. ^JH NMR (400 MHz, CDCI₃) δ Dppm 7.66 (s, 1H), 7.32 (s, 2 H), 7.16 (m, 1 H), 7.05 (m, 3 H), 4.55 (d, .7=15.3 Hz, 1 H), 4.37 (m, 1 H), 4.18 (d, .7=9.0 Hz, 1 H), 3.38 (m, 2 H), 3.27 (m, 2H), 3.08 (m, 2H), 2.85 (s, 3 H), 2.44 (s, 3 H), 2.41 (m, 2 H), 2.16 (m, 1 H), 1.97 (m, 1 H), 1.65 (q, .7=11.0 Hz, 1 H), 1.10 (m, 1 H). HPLC-MS: Rt=1.16 min, m/z (ES+): 530.03 [M + H] ⁺ .

Example 49: Compound 49

N-- r3,5-bis(trifluoromethyl^')phenyl1methyl -7-(hvdroxymethyl^')-N-methyl-l-(2- methyl phenyl)-octahvdropyrrolori,2-a1 pi perazine-2-carboxamide

(enantiomeric pair, ANTI at Cl-C8a, diastereoisomer 2)

Separation by HPLC chromatography of Intermediate 38 provided 9.8 mg of the title compound. Column: X Bridge C-18 BOD (19 x 100 mm), 5μ Mobile phase: Ammonium Bicarbonate, pH + 10, 10 mM/ACN 80/20% v/v>25/75 in 10 min> 0/100 in 1 min. Flow rate 17 mL/min Detection: DAD at 225 nm. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.65 (s, 1H), 7.32 (s, 2H), 7.16 (d, .7=2.0 Hz, 1H), 7.05 (s, 3H), 4.55 (d, .7=14.9 Hz, 1H), 4.37 (m, 1H), 4.20 (d, .7=9.4 Hz, 1H), 3.59 (dd, .7=10.6, 4.3 Hz, 1H), 3.46 (dd, .7=11.0, 6.3 Hz, 1H), 3.28 (m, 1H), 3.07 (m, 2H), 2.97 (d, .7=10.5 Hz, 1H), 2.85 (s, 3H), 2.46 (s, 3H), 2.34 (m, 2H), 2.13 (m, 2H), 1.53 (br s, 1H), 1.28 (m, 1H). HPLC-MS: Rt=1.22 min, m/z (ES+): 530.03 [M + H] ⁺ . Example 50: Compound 50

N-- r3,4-bis(tnfluoromethyl^')phenyl1methyl -N-methyl-l-(2-methylphenyl^')-7-(morpholin- 4-ylmethyl)-6-oxa-octahvdropyrrolori,2-a1piperazine-2-ca rboxamide

(enantiomer 2 of diastereoisomer 2, single isomer^')

Compound 41 (67mg) was treated with NaOH IN and the free base was extracted several times with DCM. After evaporation of the organic phase 60 mg of a pale yellow foam were obtained. Separation by chiral chromatography provided 33 mg of the title compound (6mg of a previously prepared batch of the same compound were also added) to obtain 39 mg of Compound 50 as a white solid. Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/Ethanol 70/30% v/v Flow rate: 0.8 mL/min Detection: DAD at 220 nm. Rt= 9.2. ^JH NMR (400 MHz, CDCI₃) δ ppm 7.74 (s, 1H), 7.36 (s, 2H), 7.28 (m, 1H), 7.17 (m, 3H), 4.69 (d, .7=15.7 Hz, 1H), 4.35 (d, .7=15.7 Hz, 1H), 4.21 (m, 1H), 4.06 (d, .7=9.8 Hz, 1H), 3.77 (m, 1H), 3.64 (m, 4H), 3.34 (m, 1H), 3.15 (td,

.7=12.3, 3.7 Hz, 1H), 2.94 (m, 4H), 2.71 (m, 2H), 2.52 (s, 3H), 2.41 (m, 5H), 1.89 (m, 1H), 1.79 (m, 1H). HPLC-MS: Rt=1.22; m/z (ES+): 613 [M + H] ⁺ . Example 51: Compound 51

N-- r3,4-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)-7-(morpholin-

4-ylmethyl)-6-oxa-octahvdropyrrolori,2-a1piperazine-2-ca rboxamide

(enantiomer 1 of diastereoisomer 1, single isomer)

Separation by HPLC chromatography of Compound 38 provided 35 mg of the title compound as a white solid. H NMR (400 MHz, CDCI₃) δϋ ppm 7.74 (s, 1H), 7.37 (s, 2H), 7.18 (m, 4H), 4.68 (d, .7=15.7 Hz, IH), 4.36 (d, .7=15.7 Hz, IH), 4.16 (d, .7=13.2 Hz, IH), 4.06 (d, 7=9.8 Hz, IH), 3.67 (m, 5H), 3.39 (d, 7=11.7 Hz, IH), 3.15 (td, 7=1.0 Hz, IH), 2.94 (m, IH), 2.94 (s, 3H), 2.85 (dd, 7=12.2, 3.4 Hz, IH), 2.56 (s, 3H), 2.49 (m, 6H), 2.02 (m, 7=13.0, 7.9, 7.9 Hz, IH), 1.67 (m, 7=13.0, 8.7, 8.7 Hz, IH). HPLC- MS: Rt=1.22; m/z (ES+): 613 [M + H] ⁺ . Column: Chiralpak AD-H (25 x 0.46 cm), 5μ Mobile phase: n-Hexane/2-Propanol 88/12 v/v Flow rate: 1 mL/min Detection: DAD at 220 nm. Rt= 11.9.

Example 52: Compound 52

N-- r3,5-bis(tnfluoromethyl^')phenyl1methyl -7-(hvdroxymethyl^')-N-methyl-l-(2- methylpheny0-octahydropyrrolo[l,2-a1piperazine-2-carboxamide; methanesulfonic acid salt

(single enantiomer with ANTI configuration at Cl-C8a)

Compound 28 (96 mg) was treated with DCM (20 mL) and NaHC0₃ aq sat. sol. (20 mL). The organic layer was separated, dried over sodium sulphate, filtered and evaporated under vacuo to give the title compound as a white solid (75 mg). Chiral preparative HPLC: Column: Chiralpak AD-H (25 x 0.46 cm), 5 urn; Mobile phase: n-Hexane/2- Propanol 90/10 % v/v; Flow rate (mL/min): 1.0; DAD: 220 nm; 100 % e.e. UV

(Rt=14.87 min). ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.73 (s, IH), 7.40 (s, 2H), 7.15 (m, 4H), 4.63 (d, 7=15.2 Hz, IH), 4.44 (m, IH), 4.28 (d, 7=9.3 Hz, IH), 3.66 (dd, 7=10.3, 4.4 Hz, IH), 3.54 (dd, 7=10.0, 5.6 Hz, IH), 3.35 (m, IH), 3.14 (m, 2H), 3.05 (dd, 7=8.8, 1.0 Hz, IH), 2.93 (s, 3H), 2.54 (s, 3H), 2.42 (m, 2H), 2.22 (m, 2H), 1.61 (m, IH), 1.36 (m, IH). UPLC/MS Electrospray (ES+/ES-); Rt=1.21 min a/a. (ES+): 530.2 [M + H] ⁺ .

Example 53: Compound 53

N-r(lR)-l-r3,5-bis(trifluoromethyl^')phenyl1ethyl1-7,7-bis(2-hvdroxyethyl^')-N-methyl-l- (2-methylphenv0-6-oxo-octahvdropyrrolori,2-a1piperazine-2-ca rboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

300 mg of Compound Intermediate 41 were purified by chiral preparative HPLC obtaining two fractions. After evaporation two products were obtained : diasteroisomer 1 (Compound 53, described here) and diasteroisomer 2 (Compound 54, described below). Compound 53 : white foam, 160 mg. Chiralpak IC column (25 x 0.46 cm), 5μιη. Mobile phase: n-Hexane/Ethanol; 73/27 v/v, Flow rate: 0.8 mL/min. Detection : DAD at 220 nm. Rt= 13.3 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.64 (s, IH), 7.27 (s, 2H), 7.16 (d, .7=7.3 Hz, IH), 7.07 (m, 3H), 5.51 (q, 7=7.3 Hz, IH), 4.07 (d, 7= 12.7 Hz, IH), 3.99 (d, 7=9.8 Hz, IH), 3.71 (m, 4H), 3.53 (m, IH), 3.27 (m, IH), 3.07 (td, 7= 12.7, 5.9 Hz, IH), 2.88 (td, 7= 12.2, 3.4 Hz, IH), 2.88 (br. s, IH), 2.74 (s, 3H), 2.46 (s, 3H), 2.00 (br. s, IH), 1.74 (m, 6H), 1.43 (d, 7=6.8 Hz, 3H).

Example 54: Compound 54

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7,7-bis(2-hvdroxyethyl)-N-methyl-l-2- methylphenyl)-6-oxo-octahvdropyrrolor i ,2-a1piperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Compound 54: white foam 120 mg. Chiralpak IC column (25 x 0.46 cm), 5μιη. Mobile phase: n-Hexane/Ethanol; 73/27 v/v, Flow rate: 0.8 mL/min. Detection : DAD at 220 nm. Rt= 16.2 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.70 (s, IH), 7.46 (s, 2H), 7.17 (d, 7=8.3 Hz, IH), 7.10 (m, 3H), 5.47 (quin, 7=5.0 Hz, IH), 4.06 (d, 7= 12.7 Hz, IH), 3.99 (d, 7=9.8 Hz, IH), 3.75 (m, 3H), 3.64 (m, IH), 3.52 (m, IH), 3.22 (d, 7= 10.8 Hz, IH), 3.06 (td, 7= 13.7, 2.9 Hz, IH), 2.94 (td, 7= 12.2, 2.0 Hz, IH), 2.86 (m, IH), 2.62 (s, 3H), 2.46 (s, 3H), 1.99 (m, IH), 1.75 (m, 6H), 1.33 (d, 7=6.8 Hz, 3H). [M + H]+ CALC:

616.2610; OBS : 616.2601 Example 55: Compound 55

N-rflRI-l-rS.S-bisftnfluoromethvnphenyllethyll-y-fhvdroxymethvn-N-methyl-l-f - methylphenvn-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Intermediate 47 (300mg) was separated in the corresponding isomers by chiral chromatography. After evaporation of collected fraction from chiral preparative HPLC, Compound 55 was obtained (isomer 1, 56 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/Ethanol 85/15%v/v, Flow rate: 0.8 mL/min. Detection: DAD at 220 nm, Rt = 22.5 min. ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.71 (s, IH), 7.47 (s, 2H), 7.16 (d, J = 7.8 Hz, IH), 7.08 (m, 3H), 5.47 (q, J = 6.8 Hz, IH), 4.11 (d, J = 12.2Hz, IH), 3.99 (d, J=9.8 Hz, IH), 3.78 (m, IH), 3.70 (m, IH), 3.59 (m, IH), 3.16 (d, 3 = 11.7 Hz, IH), 3.09 (td, J = 13.2, 3.9 Hz, IH), 2.88 (td, J = 12.2, 3.4Hz, IH), 2.68 (m, IH), 2.63 (s, 3H), 2.46 (s, 3H), 2.44 (dd, J = 7.8, 3.9 Hz, IH), 1.74 (m, IH), 1.65 (m, J = 5.9 Hz, IH), 1.32 (q, J = 6.8 Hz, 3H). Example 56: Compound 56

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7-(hvdroxymethyl)-N-methyl-l-(2- methylphenyl)-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

After evaporation of the second collected fraction from chiral preparative HPLC,

Compound 56 was obtained (isomer 2, 172 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/Ethanol 85/15%v/v , Flow rate: 0.8 mL/min. Detection : DAD at 220 nm, 99.4% a/a by UV Rt=24.5 min. ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.70 (s, 1H), 7.47 (s, 2H), 7.17 (d, J = 7.8 Hz, 1H), 7.09 (m, 3H), 5.47 (q, J = 6.7 Hz, 1H), 4.07 (d, J = 12.7Hz, 1H), 4.01 (d, J=9.8 Hz, 1H), 3.83 (m, 1H), 3.67 (m, 2H), 3.22 (d, J = 10.8 Hz, 1H), 3.06 (t, J = 12.7 Hz, 1H), 2.90 (m, 2H), 2.62 (s, 3H), 2.55 (m, 1H), 2.46 (s, 3H), 1.88 (m, 1H), 1.43 (m, 1H), 1.33 (d, J = 7.3 Hz, 3H).

Example 57: Compound 57

N-r(lR)-l-r3,5-bis(tnfluoromethyl^')phenyl1ethyl1-7-(hvdroxymethyl^')-N-methyl-l-(2- methyl phenvn-6-oxo-octahvdropyrrolor i ,2-a1 pi perazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Intermediate 48 (350mg) was separated in the corresponding isomers by chiral chromatography. After evaporation of collected fraction from chiral preparative HPLC, Compound 57 was obtained (isomer 1, 199 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v , Flow rate: 1 mL/min.

Detection : DAD at 220 nm, Rt=7 min ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.72 (br s, 1H), 7.36 (br s, 2H), 7.23 (d, J = 7.3 Hz, 1H), 7.15 (m, 3H), 5.58 (m, 1H), 4.17 (d, J = 12.7 Ηζ,ΙΗ), 4.09 (d, J=9.8 Hz, 1H), 3.91 (m, 1H), 3.74 (m, 1H), 3.69 (q, J = 7.3 Hz, 1H), 3.35 (d, J = 12.2 Hz, 1H), 3.15 (m, 1H), 2.97 (m, 2H), 2.82 (s, 3H), 2.64(m, 1H), 2.53 (s, 3H), 1.94 (m, 1H), 1.55 (m, 1H), 1.51 (d, J =6.8 Hz, 3H).

Example 58: Compound 58 N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7- (hvdroxymethyl)-N-methyl-l-(2-methylphenyl)-6-oxo-octahvdropyrrolor i,2- alpiperazine-2-ca rboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Compound 58 was obtained (isomer 2, 49.5 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v , Flow rate: 1 mL/min.

Detection : DAD at 220 nm, Rt=8.6 min. ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.72 (br s, IH), 7.35 (s, 2H), 7.23 (d, J = 7.3 Hz, IH), 7.16 (m, 3H), 5.58 (m, IH), 4.21 (d, J = 13.2 Hz, IH), 4.06 (d, J = 10.3 Hz, IH), 3.86 (m, IH), 3.74 (m, IH), 3.67 (m, IH), 3.30 (d, J = 12.2 Hz, IH), 3.19 (m, IH), 2.91 (m, IH), 2.82 (s, 3H), 2.76 (m, 1H),2.52 (m, 4H), 1.83 (m, IH), 1.71 (m, IH), 1.51 (d, J = 6.8 Hz, 3H).

Example 59: Compound 59 N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl1ethyll-7,7-bis(2- hydroxyethyl)-N-methyl-l-(2-methylphenyl)-octahydropyrrolo[ l ,2-alpiperazine-2- ca rboxamide

(pure enantiomer, isomer 1, with ANTI configuration at Cl-C8a)

620 mg of Intermediate 42 were purified by chiral preparative HPLC obtaining two fractions. After evaporation, two products were obtained : diasteroisomer 1 (Compound 59, described here) and diasteroisomer 2 (Compound 60, described below). Compound 59: white foam, 166 mg . Chiral HPLC: Chiralpak IC column (25 x 0.46 cm), 5μιη. Mobile phase: n-Hexane/Ethanol 85/15 v/v, Flow rate: 0.8 mL/min. Detection : DAD at 220 nm. Rt= 14.3 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.62 (s, IH), 7.29 (s, 2H), 7.13 (m, IH), 7.04 (m, 3H), 5.51 (q, 7=7.3 Hz, IH), 4.97 (br s, 2H), 4.27 (d, 7= 10.8 Hz, IH), 3.83 (td, 7=9.8, 2.4 Hz, IH), 3.68 (s, IH), 3.57 (d, 7=4.4 Hz, 2H), 3.26 (d, 7= 12.7 Hz, IH), 3.04 (m, 3H), 2.70 (s, 3H), 2.48 (s, 3H), 2.39 (m, 2H), 2.13 (d, 7=9.3 Hz, IH), 1.73 (m, IH), 1.64 (t, 7= 12.2 Hz, IH), 1.55 (t, 7=7.8 Hz, 2H), 1.42 (d, 7=6.8 Hz, 3H), 1.36 (m, IH), 1.16 (dd, 7= 13.7, 5.4 Hz, IH). Example 60: Compound 60 N-ri l RM- r3,5-bis(tnfluoromethvn

hvdroxyethyl^')-N-methyl- l-(2-methylphenyl^')-octahvdropyrrolor i ,2-a1piperazine-2- ca rboxamide

(pure enantiomer, isomer 2, with ANTI configuration at Cl-C8a)

Compound 60: white foam 160 mg. Chiral HPLC: Chiralpak IC column (25 x 0.46 cm), 5μιη. Mobile phase: n-Hexane/Ethanol 85/15 v/v, Flow rate: 0.8 mL/min. Detection : DAD at 220 nm. Rt= 17.3 min. ^JH NMR (500 MHz, CDCI₃) δ ppm 7.77 (s, IH), 7.56 (s,

2H), 7.21 (d, 7=7.8 Hz, IH), 7.13 (m, 3H), 5.53 (q, 7=6.8 Hz, IH), 4.95 (br s, 2H), 4.35 (d, 7=8.8 Hz, IH), 3.91 (m, IH), 3.75 (m, IH), 3.64 (d, 7=3.9 Hz, 2H), 3.28 (d, 7= 12.2 Hz, IH), 3.11 (d, 7=8.8 Hz, 3H), 2.67 (br s, 3H), 2.58 (s, 3H), 2.45 (m, 2H), 2.20 (d, 7=8.3 Hz, IH), 1.81 (m, IH), 1.70 (dd, 7= 13.7, 10.5 Hz, IH), 1.63 (t, 7=7.3 Hz, 2H), 1.41 (br s, 4H), 1.23 (dd, 7= 12.7, 8.3 Hz, IH). [M + H]+ CALC: 602.2812; OBS :

602.2814.

Example 61 : Compound 61

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -N-methyl-l-(2-methylphenyl)- octahvdropyrrolor i,2-a1 pi perazine-2-ca rboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Compound 24 was separated in the corresponding isomers by chiral chromatography. After evaporation of collected fractions from chiral preparative HPLC, two isomers were obtained (isomer 1, described here and isomer 2, described in the next experimental part). Isomer 1 (15.5 mg) : Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v , Flow rate: 1 mL/min. Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt=3.9 min ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.73 (s, IH), 7.41 (s, 2H), 7.15 (m, 4H), 4.63 (d, J = 15.7 Hz, IH), 4.46 (m, IH), 4.26 (d, J=9.3 Hz, 1H),3.38 (m, IH), 3.18 (m, 3H), 2.93 (s, 3H), 2.52 (s, 3H), 2.47 (m, IH), 2.22 (q, J=9.1 Hz, IH), 2.14 (m, IH), 1.82 (m, IH), 1.58 (m, 2H), 1.39 (m, IH).

Example 62: Compound 62

Ν--Γ [3, 5-bis(trifluoromethyl) phenyl] methyl -N-methyl- l-(2-methyl phenyD- octahydropyrrolo[ l,2-alpiperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

After evaporation of the second collected fraction from chiral preparative HPLC as described in the previous experimental, Compound 62 was obtained (isomer 2, 16.7 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v , Flow rate: 1 mL/min. Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt=5.4 min ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.73 (s, IH), 7.41 (s, 2H), 7.15 (m, 4H), 4.63 (d, J = 15.7 Hz, IH), 4.46 (m, IH), 4.26 (d, J=9.3 Hz, 1H),3.38 (m, IH), 3.18 (m, 3H), 2.93 (s, 3H), 2.52 (s, 3H), 2.47 (m, IH), 2.22 (q, J=9.1 Hz, IH), 2.14 (m, IH), 1.82 (m, IH), 1.58 (m, 2H), 1.39 (m, IH).

Example 63 : Compound 63

N-[(lR)-l-[3,5-bis(trifluoromethynphenyl1ethyll-N-methyl-l-(2-methylphenyl)- octahvdropyrrolor i,2-a1piperazine-2-carboxamide

(pure enantiomer, isomer 1, with ANTI configuration at Cl-C8a)

Intermediate 43 was purified by chiral preparative HPLC. After evaporation of collected fractions from chiral preparative HPLC, Compound 63 was obtained (isomer 1, 101.1 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v , Flow rate: 1 mL/min. Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt=3.9 min. ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (s, IH), 7.36 (s, 2 H), 7.20 (m, 3H), 4.68 (d, J = 15.7 Hz, IH), 4.34 (d, J = 15.7 Hz, IH), 4.17 (dt, J = 13.7, 2.7 Hz, IH), 4.02 (d, J=9.8 Hz, IH), 3.67 (dt, J=9.4, 7.4 Hz, IH), 3.36 (dt, J = 11.7, 2.7 Hz, IH), 3.14 (td, J = 11.7, 3.1 Hz, IH), 2.95 (td, J = 11.7,3.5 Hz, IH), 2.95 (s, 3H), 2.83 (m, IH), 2.69 (m, IH), 2.52 (s, 3H), 2.24 (s, 3H), 2.20 (m, IH), 1.91 (m, 4H), 1.46 (m, 2H), 1.33 (m, IH) .

Example 64: Compound 64

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-N-methyl-l-(2-methylphenyl)- octahvdropyrrolor i,2-a1piperazine-2-carboxamide

(pure enantiomer, isomer 2, with ANTI configuration at Cl-C8a)

After evaporation of the second collected fraction from chiral preparative HPLC

Compound 64 was obtained (isomer 2, 150 mg). Chiral HPLC: Chiralpak AD-H column (25 x 0.46 cm), 5μιη, n-Hexane/2-propanol 90/10%v/v; Flow rate: 1 mL/min.

Detection : DAD at 220 nm, Circular Dichroism detector: 230nm, Rt=3.9 min. H NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (s, IH), 7.36 (s, 2H), 7.20 (m, 3H), 4.68 (d, J = 15.7 Hz, IH), 4.34 (d, J = 15.7 Hz, IH), 4.17 (dt, J = 13.7, 2.7 Hz, IH), 4.02 (d, J=9.8 Hz, IH), 3.67 (dt, J=9.4, 7.4 Hz, IH), 3.36 (dt, J = 11.7, 2.7 Hz, IH), 3.14 (td, J = 11.7, 3.1 Hz, IH), 2.95 (td, J = 11.7,3.5 Hz, IH), 2.95 (s, 3H), 2.83 (m, IH), 2.69 (m, IH), 2.52 (s, 3H), 2.24 (s, 3H), 2.20 (m, IH), 1.91 (m, 4H), 1.46 (m, 2H), 1.33 (m, IH). Example 65 : Compound 65

N-- r3,5-bis(trifluoromethyl)phenyl1methyl -7,7-bis(2-hvdroxyethyl)-N-methyl-l-(2- methylphenyl)-octahvdropyrrolor i,2-a1piperazine-2-carboxamide (pure enantiomer, with ANTI confi uration at Cl-C8a)

To a 0°C cooled solution of Intermediate 49 (2.09 g, 3.47 mmol) in dry THF (30 mL) under nitrogen, a solution of BH₃.SMe₂ (2M, THF) was added (6.94 mL, 13.88 mmol) and the resulting mixture was stirred at RT 17h. The mixture was cooled again at 0°C and a second amount of BH₃.SMe₂ (2M, THF) was added dropwise (3.47 mL, 6.94 mmol) and the mixture was stirred at RT for 6h, then it was quenched by adding HCI 1M (15 mL) and MeOH (15 mL). The resulting mixture was stirred at RT for 17h, then it was concentrated in vacuo. The residue was diluted with water (50 mL) and the PH adjusted to 9 by addition of NaHC0₃ aq. sat. sol., followed by extraction with DCM (3x50 mL). The combined organic layers were dried over Na₂S0₄, filtered and concentrated in vacuo. The residue was dissolved in 15 mL of MeOH then loaded on SCX cartridge (Strata 20g, Phenomenex). The cartridge was washed with MeOH, then diluted with ammonia 2M in MeOH. After evaporation of the fractions, 1.63 g of a white solid were obtained. This material was purified by chiral preparative HPLC (Column :Chiralpak IC (25 x 3.0 cm), 5 μ; Mobile phase: n-Hexane/2-Propanol 90/10 % v/v; Flow rate (ml/min)

32 ml/min; DAD detection 220 nm) to give two fractions, which, after evaporation gave two products: Enantiomer 1 (Compound 65, described here) and enantiomer 2

(Compound 66, described below). Compound 65 (529 mg) : (Column Chiralpak IC (25 x 0.46 cm), 5 um; Mobile phase n-Hexane/Ethanol 85/15 % v/v; Flow rate (ml/min) 0.8; DAD 220 nm; CD 230 nm;) Rt= 13.973 min., m/z (ES+) : 588.3 [M + H] ⁺ ; ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (s, 2H), 7.38 (s, 3H), 7.24 (m, 2H), 7.13 (m, 4H), 5.02 (br s, 2H), 4.66 (m, 2H), 4.43 (br s, 2H), 4.35 (d, 2H), 3.91 (td, 2H), 3.75 (m, 2H), 7.65 (m, 3H), 3.37 (m, 2H), 3.14 (m, 5H), 2.92 (s, 4H), 2.56 (s, 4H), 2.46 (m, 4H), 2.20 (d, 2H), 1.81 (m, 2H), 1.71 (dd, 2H), 1.63 (t, 3H), 1.44 (m, 3H).

Example 66: Compound 66

"N-r[3,5-bis(trifluoromethyl)phenyl1methyl -7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-alpiperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Compound 66 (Enantiomer 2) : (Column Chiralpak IC (25 x 0.46 cm), 5 um; Mobile phase n-Hexane/Ethanol 85/15 % v/v; Flow rate (ml/min) 0.8; DAD 220 nm; CD 230 nm;) Rt= 19.318 min., m/z (ES+) : 588.2 [M + H] ⁺ ; ^JH NMR (400 MHz, CHLOROFORM-d) δ ppm 7.73 (m, IH), 7.38 (s, 2H), 7.27 (s, 2H), 7.15 (d, 3H), 5.02 (m, IH), 4.64 (d, IH), 4.39 (m, IH), 4.38 (m, IH), 4.35 (d, 2H), 3.91 (m, IH), , 3.76 (m, IH), 3.63 (m, 2H), 3.37 (m, IH), 3.14 (s, 3H), 2.92 (s, 3H), 2.56 (s, 3H), 2.46 (m, 2H), 2.20 (d, IH), 1.81 (m, IH), 1.70 (m, IH), 1.63 (t, 2H), 1.44 (m, 2H). 1.23 (m, IH).

Examble 67: Combound 67

N-r(lR)-l-r3,5-bis(tnfluoromethyl)bhenyl1ethyl1-7-(hvdroxymethyl)-N-methyl-l-(2- methylbhenyl)-octahvdrobyrrolor i,2-a1biberazine-2-carboxamide

(isomer 1, pure enantiomer, with ANTI configuration at Cl-C8a)

CaCI₂ (226.4 mg, 2.04 mmol) was added to a solution of Intermediate 44 (0.8 g, 1.36 mmol) in MeOH (40 mL), then it was cooled at 0°C and NaBH₄ (154.3 mg, 4.08 mmol) was added portionwise. After stirring at 25°C for 0.5h, water (20 mL) was added, MeOH was evaporated and the aqueous layer was extracted with DCM (3x50 mL). The organic layer was separated, dried over Na₂S0₄, filtered and evaporated to give 0.7g of a yellow oil. The same reaction was repeated on a different batch of starting material to give other 0.5 g of a yellow oil. Both crudes were purified by preparative HPLC (Fractionlynx (Waters) with ZQ MS detector; LC/MS Conditions: Columns: Phenomenex Luna C18 (2) 250 x 21.2 mm 10; μιη @ RT; Solvents: H20 + 0.1 % HCOOH; Acetonitrile; UV detection range: 210 nm to 350 nm; Acquisition rate: 1.0 spectra/s) to give three fractions each ; Rt= 13.98 min (fraction A), Rt= 14.32 min (fraction B), Rt= 15.22 min (fraction C) . Both chromatograms showed peaks having the same Rt, thus, the corresponding fractions were combined together. Fractions A (95 mg, containing mainly one isomer) . Fraction B (200 mg, containing mainly two isomers) and Fraction C ( 120 mg, containing mainly one isomer) . Elaboration of Fractions B and C will be described in the three next experimental parts. Fraction A (95 mg) was dissolved in dry THF ( 10 mL) and, at 0°C, BH₃. Me₂S (2 M in THF) (0.34 mL, 0.68 mmol) was added d ropwise. The reaction mixture was stirred at RT for 16 h . BH₃. Me₂S (2 M in THF) (0.34 mL, 0.68 mmol) was added again and the reaction was left stirring at RT for 8h . MeOH (2 mL) was added dropwise followed by HCI I N (2 mL) and the reaction mixture was stirred overnight at RT, then it was concentrated in vacuo, diluted with DCM (30 mL) and washed with NaHC0₃ aq . sat. sol . (20 mL) . The organic layer was separated, dried over Na₂S0₄, filtered and concentrated in vacuo to give 85 mg of a colourless oil which was purified by preparative HPLC (Rt= 1.9 min) . After evaporation of the fractions, the title compound (33.9 mg) was obtained as a white solid . HPLC-MS : Rt= 1.20 min, m/z (ES+) : 544.2 [M + H] ⁺ . ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.78 (s, 1 H), 7.58 (s, 2H), 7.13 (m, 4H), 5.56 (d, .7=6.8 Hz, 1H), 4.26 (d, .7=9.3 Hz, 1 H), 3.46 (m, 2H), 3.32 (m, 2H), 3.15 (m, 2H), 2.68 (s, 3H), 2.54 (s, 3H), 2.47 (m, 2H), 2.24 (d, .7= 5.9 Hz, 1H), 2.04 (t, .7=8.6 Hz, 1 H), 1.73 (m, 1 H), 1.41 (d, .7=6.4 Hz, 3H), 1.17 (td, .7=6.4, 2.9 Hz, 1 H) .

Exa mple 68 : Compound 68

N-r( lR)- l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7-(hvdroxymethyl)-N-methyl- l-(2- methylphenyl)-octahvdropyrrolor i ,2-a1 piperazine-2-carboxamide

(isomer 2, pure enan l-C8a)

Fraction B mentioned in Example 67 (200 mg) was dissolved in dry THF (25 mL) and, at 0°C, BH₃. Me₂S (2 M in THF) (0.7 mL, 1.4 mmol) was added d ropwise. The reaction mixture was stirred at RT for 16 h . BH₃. Me₂S (2 M in THF) (0.7 mL, 1.4 mmol) was added again and the reaction was left stirring RT for 8h . MeOH (2 mL) was added dropwise followed by HCI I N (2 mL) and the reaction mixture was stirred overnight at RT, then it was concentrated in vacuo, diluted with DCM (30 ml_) and washed with NaHC0₃ aq. sat. sol. (20 ml_). The organic layer was separated, dried over Na₂S0₄, filtered and concentrated in vacuo to give 180 mg of a colourless oil which was purified by preparative HPLC (LC/MS System: Fractionlynx (Waters) with ZQ MS detector LC/MS Conditions: Columns: Gemini 5 μιη C18110A AXIA 100 x 30 mm; Injection loop: 1 ml; Solvents: ammonium bicarbonate acqueous solution adjusted to pH 10 with ammonia, Acetonitrile; UV detection range: 210 nm to 350 nm; Rt=10.86 min and 11.95 min). After evaporation of the fractions, two isomers were isolated. Isomer 2 (described here) and isomer 3 (described below). The title compound (24 mg) was obtained as a white solid. HPLC-MS: Rt=1.22 min, m/z (ES+): 544.2 [M + H] ⁺ . ^JH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.71 (s, IH), 7.39 (s, 2H), 7.14 (m, 4H), 5.61 (d, 7=6.8 Hz, IH), 4.25 (d, 7=9.8 Hz, IH), 3.47 (dd, 7=10.3, 6.8 Hz, 2H), 3.35 (m, 2H), 3.15 (m, 2H), 2.79 (s, 3H), 2.48 (m, 5H), 2.24 (m, IH), 2.05 (t, 7=8.6 Hz, IH), 1.75 (m, IH), 1.51 (d, 7=6.8 Hz, 3H), 1.18 (m, IH).

Example 69: Compound 69

N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7-(hvdroxymethyl)-N-methyl-l-(2- methylphenyl)-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(isomer 3, pure enantiomer, with ANTI configuration at Cl-C8a)

Compound 69 (Isomer 3 mentioned in the experimental of Compound 68) was obtained as a white solid (45.7 mg mg). HPLC-MS: Rt=1.26 min, m/z (ES+): 544.0 [M + H] ⁺ . IH NMR (500 MHz, CHLOROFORM-d) δ ppm 7.74 (s, IH), 7.37 (s, 2H), 7.26 (m, IH), 7.16 (m, 3H), 4.69 (d, 7=15.7 Hz, IH), 4.36 (d, 7=15.4 Hz, IH), 4.18 (dt, 7=12.8, 2.8 Hz, IH), 4.09 (d, 7=10.0 Hz, IH), 3.73 (dt, 7=9.7, 7.4 Hz, IH), 3.37 (dt, 7=12.2, 2.8 Hz, IH), 3.15 (td, 7=12.5, 2.7 Hz, IH), 2.96 (s, 3H), 2.96 (m, IH), 2.53 (s, 3H), 2.44 (m, IH), 2.35 (m, IH), 1.87 (dddd, 7=13.2, 9.6, 7.3, 3.9 Hz, IH), 1.69 (m, IH).

Example 70: Compound 70 N-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-7-(h^

methyl phenyl)-octahvdropyrrolori,2-a1 pi perazine-2-carboxamide

(isomer 4, pure enantiomer, with ANTI configuration at Cl-C8a)

Fraction C mentioned in Example 67 (120 mg) was dissolved in dry THF (15 mL) and, at 0°C, BH₃.Me₂S (2 M in THF) (0.42 mL, 0.84 mmol) was added dropwise. The reaction mixture was stirred at RT for 16 h. BH₃.Me₂S (2 M in THF) (0.42 mL, 0.84 mmol) was added again and the reaction was left stirring RT for 8h. MeOH (2 mL) was added dropwise followed by HCI IN (2 mL) and the reaction mixture was stirred overnight at RT, then it was concentrated in vacuo, diluted with DCM (30 mL) and washed with NaHC0₃ aq. sat. sol. (20 mL). The organic layer was separated, dried over Na₂S0₄, filtered and concentrated in vacuo to give 120 mg of a colourless oil which was purified by chiral preparative HPLC (Column Chiralpak IC (25 x 3.0 cm), 5 μ; Mobile phase: n- Hexane/2-Propanol 90/10 % v/v; Flow rate (ml/min): 40 ml/min; DAD detection: 220 nm, Rt= 10.86 min). After evaporation of the fractions, the title compound (48.6 mg) was obtained as a white solid. Column: Chiralpak IC (25 x 0.46 cm), 5 um; Mobile phase: n-Hexane/2-Propanol 90/10 % v/v; Flow rate (ml/min): 1.0; DAD: 220 nm; Rt=12.83; Rt=1.28 min, m/z (ES+): 544.5 [M + H] ⁺ . ^JH NMR (500 MHz, CHLOROFORM- d) δ ppm 7.70 (s, IH), 7.38 (s, 2H), 7.13 (m, 4H), 5.61 (q, 7=6.8 Hz, IH), 4.28 (d, 7=9.3 Hz, IH), 3.67 (dd, 7=10.0, 4.6 Hz, IH), 3.54 (dd, 7=10.0, 5.6 Hz, IH), 3.32 (m, IH), 3.09 (m, 3H), 2.79 (s, 3H), 2.54 (s, 3H), 2.42 (m, 2H), 2.22 (m, 2H), 1.60 (m, IH), 1.51 (d, 7=7.3 Hz, 3H), 1.37 (ddd, 7=12.5, 10.5, 5.9 Hz, IH).

Example 71: Compound 71

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl1ethyll-N-methyl-l-(2-methylphenyl)-7- (morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a) To a solution of Intermediate 50 (2.31 g, 3.64 mmol) in dry THF (60 mL) was added morpholine (3.18 mL, 36.4 mmol) and the reaction mixture was stirred at 65°C for 4 days. The mixture was allowed to cool to RT and the solvent was removed in vacuo. The residue was partitioned between EtOAc (50 mL) and NaHC0₃ aq . sat. sol . (40 mL), then dried over Na₂S0₄, filtered and concentrated in vacuo. The residue was dissolved in 8 mL of MeOH and loaded on a SCX cartridge (Strata 20 g, Phenomenex) . Elution with ammonia 2M in MeOH a nd evaporation of the fractions provided 1.7 g of a crude as a pale orange oil . This crude was separated via chiral preparative HPLC, (Column Chiralpak AD-H (25 x 3.0 cm), 5 μ Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 40 ml/min DAD detection 220 nm Loop 1000 μί Total amount 1743 mg

Solubilization 1743 mg in 58 ml EtOH/n-Hexane 7/3 = 30 mg/ml), providing 3 fractions. The first collected fraction resulted in a mixture of two isomers, while the second one and the third one contained pure isomers. The second fraction was evaporated, to provide 220 mg of the title compound as a white solid . H NMR (500 MHz, CDCI₃) δ ppm 7.72 (s, 1 H), 7.35 (s, 2H), 7.18 (m, 4H), 5.58 (q, .7=7.2 Hz, 1 H), 4.21 (d, .7= 13.2 Hz, 1 H), 4.04 (d, .7= 10.3 Hz, 1H), 3.74 (m, 1H), 3.64 (m, 4H), 3.29 (d, .7= 12.2 Hz, 1H), 3.14 (td, .7= 12.5, 3.9 Hz, 1H), 2.90 (td, .7= 12.0, 2.9 Hz, 1 H), 2.82 (s, 3H), 2.73 (dt, .7=9.3, 4.6 Hz, 1H), 2.69 (m, 1H), 2.52 (s, 3H), 2.47 (m, 2H), 2.41 (m, 1 H), 2.37 (m, 2H), 1.88 (m, 1 H), 1.80 (m, 1H), 1.51 (d, -7=7.3 Hz, 3H) . Chira l HPLC: 18.7 min Column Chiralpak AD-H (25 x 0.46 cm), 5 urn Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 1.0 DAD 220 nm CD - nm Loop 20 μί . UPLC-MS : Rt= 1.27; m/z (ES+) : 627.2 [M + H] ⁺ .

Exa mple 72 : Compound 72

N-r( lR)- l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-N-methyl- l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahvdropyrrolor i ,2-a1 piperazine-2-carboxa mide

(pure enantiomer, with ANTI configuration at Cl-C8a)

Evaporation of the third fraction provided 411 mg Compound 72 as a white solid. ¹ NMR (500 MHz, CDCI₃) δ ppm 7.72 (s, IH), 7.35 (s, 2H), 7.18 (m, 4H), 5.59 (q, 7=7.3 Hz, IH), 4.15 (m, IH), 4.05 (d, 7=9.8 Hz, IH), 3.66 (m, 5H), 3.34 (m, IH), 3.14 (td, 7=12.5, 2.9 Hz, IH), 2.91 (td, 7=12.1, 3.2 Hz, IH), 2.85 (dd, 7=12.0, 3.7 Hz, IH), 2.82 (s, 3H), 2.58 (m, 4H), 2.52 (m, IH), 2.47 (m, 2H), 2.42 (m, 2H), 2.01 (m, IH), 1.68 (dt, 7=13.1, 8.6 Hz, IH), 1.51 (d, 7=7.3 Hz, 3H). Chiral HPLC: 27.1 min Column

Chiralpak AD-H (25 x 0.46 cm), 5 urn Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 1.0 DAD 220 nm CD - nm Loop 20 μΙ_. UPLC-MS: Rt=1.26; m/z (ES+): 627.2 [M + H] ⁺ .

Example 73: Compound 73

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl1ethyll-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[l,2-alpiperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

The first fraction was subjected to a further purification by preparative chiral HPLC (Column Chiralpak AD-H (25 x 3.0 cm), 5 μ Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 40 ml/min DAD detection 220 nm Loop 1000 μί Total amount 600 mg Solubilization 600 mg in 30 ml EtOH/n-Hexane 2/1 = 20 mg/ml), providing two fractions. The first fraction eluted was evaporated, providing 157 mg of Compound 73 as a white solid. H NMR (500 MHz, CDCI₃) δ ppm 7.78 (s, IH), 7.55 (s, 2H), 7.18 (m, 4H), 5.56 (q, 7=7.8 Hz, IH), 4.14 (m, IH), 4.06 (d, 7=9.8 Hz, IH), 3.68 (m, 5H), 3.28 (d, 7=12.7 Hz, IH), 3.12 (td, 7=11.2, 5.4 Hz, IH), 2.97 (td, 7=13.7, 2.4 Hz, IH), 2.85 (dd, 7=13.7, 3.0 Hz, IH), 2.70 (s, 3H), 2.57 (m, 4H), 2.52 (d, 7=13.7 Hz, IH), 2.44 (m, 4H), 2.02 (m, IH), 1.65 (m, IH), 1.40 (d, 7=6.8 Hz, 3H). Chiral HPLC: Column Chiralpak AD- H (25 x 0.46 cm), 5 μ Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 1.0 DAD 220 nm Loop 20 μΙ_ 100 % e.e. (11.2 min). UPLC-MS: Rt=1.26; m/z (ES+): 627.2 [M + H] ⁺ .

Example 74: Compound 74

N-r(lR)-l-r3,5-bis(tnfluoromethyl^')phenyl1ethyl1-N-methyl-l-(2-methylphenyl^')-7- (morpholin-4-ylmethvn-6-oxo-octahvdropyrrolori,2-a1piperazine-2-carboxamide

(pure enantiomer, with ANTI configuration at Cl-C8a)

From the same purification, the second fraction eluted was evaporated, providing 34 mg of Compound 74 as a white solid. H NMR (500 MHz, CDCI₃) δ ppm 7.71 (m, IH), 7.46 (s, 2H), 7.12 (m, 4H), 5.46 (q, 7=7.3 Hz, IH), 4.11 (d, 7=12.7 Hz, IH), 3.97 (d, 7=10.3 Hz, IH), 3.71 (m, IH), 3.56 (d, 7=3.4 Hz, 4H), 3.16 (d, 7=10.8 Hz, IH), 3.04 (td, j=11.7, 4.4 Hz, IH), 2.88 (td, 7=13.0, 2.8 Hz, IH), 2.66 (m, IH), 2.62 (s, 3H), 2.60 (m, IH), 2.45 (s, 3H), 2.39 (m, 2H), 2.33 (dd, 7=12.7, 9.8 Hz, IH), 2.28 (m, IH), 1.81 (m, IH), 1.70 (m, IH), 1.32 (d, 7=6.8 Hz, 3H) Chiral HPLC: Column Chiralpak AD-H (25 x 0.46 cm), 5 μ Mobile phase n-Hexane/2-Propanol 90/10 % v/v Flow rate (ml/min) 1.0 DAD 220 nm Loop 20 μί 93.6 % e.e. (13.0 min). UPLC-MS: Rt=1.27; m/z (ES+): 627.2 [M + H] ⁺ . Example 75: Compound 75

A/-r(lR)-l-r3,5-bis(trifluoromethyl)phenyl1ethyl1-A/-methyl-l-(2-methylphenyl)-6-oxo- octahvdropyrrolori,2-a1 piperazine 2 carboxamide

(enantiomer 1, single isomer with SYN configuration at Cl-C8a)

To a solution of triphosgene (63.6 mg, 0.22 mmol) in EtOAc (2 mL) at 0 °C was added solution of l-(2-methylphenyl)-octahydropyrrolo[l,2-a]piperazin-6-one hydrochloride (racemic mixture with SYN configuration at Cl-C8a, 100 mg, 0.43 mmol), DMAP (10.4 mg, 0.09 mmol) and TEA (90 mg, 0.86 mmol) in EtOAc (2 mL). The mixture was stirred for 1.5 h, followed by addition of l-(3,5-bis(trifluoromethyl) phenyl) -N- methylmethanamine (163 mg, 0.6 mmol) in EtOAc (2 mL) and TEA (90 mg, 0.86 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 75 (20 mg, yield: 9%).¹ NMR (400 MHz, CDCI₃) δ ppm 7.80 (s, IH), 7.68 (s, 2H), 7.37 (d, .7=7.6 Hz, IH), 7.22 (m, 3H), 5.54 (d, .7=4.8 Hz, IH), 5.11 (m, IH), 4.30 (m, IH), 4.20 (m, IH), 3.45 (m, 2H), 3.02 (m, IH), 2.51 (s, 3H), 2.38 (m, 2H), 2.29 (s, 3H), 1.74 (m, IH), 1.70 (m, 3H); m/z (ES+): 528 [M + H] ⁺ . Another enantiomer (single isomer with SYN configuration at Cl- C8a, 12 mg, yield: 5%). Example 76: Compound 76

ilS,8aS)-V-i3-fluoro-5-itrifluoromethvnbenzylV7,7-bisi2-hvdroxyethylVV-methyl-6-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 56 (20 mg, 0.037 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (20 mg, 0.53 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 76 (4 mg, yield: 20%). *H NMR (400 MHz, CDCI₃) δ ppm 7.28 (s, IH), 7.21 (m, 4H), 7.04 (s, IH), 6.56 (d, .7=8.8 Hz, IH), 4.66 (d, .7=15.6 Hz, IH), 4.20 (m, IH), 4.17 (m, IH), 4.06 (m, IH), 3.80 (m, 4H), 3.60 (m, IH), 3.38 (m, IH), 3.16 (m, IH), 2.96 (m, 4H), 2.55 (s, 3H), 1.74 (m, IH), 1.80 (m, 7H). m/z (ES+): 552 [M + H] ⁺ .

Example 77: Compound 77 ( lS,8aSV7,7-bis(2-hvdroxyethylV/V-methyl-/V-(3-methyl-5-(tnfluoromethyl^')benzyl^')-6-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 57 ( 130 mg , 0.22 mmol) in DCM ( 10 ml_) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ ( 114 mg, 3.0 mmol) . The reaction mixture was allowed to wa rm to room temperature and stirred for 20 h . After quenched with water, the resulting mixture was extracted with water and the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum . The residue was purified by Prep-HPLC to give the compound 77 ( 15 mg, yield : 18.3%) . ¹ NMR (400 MHz, DMSO) δ ppm 7.40 (m, 2H), 7.15 (m, 4H), 6.87 (s, 1 H), 4.35 (m, 4H), 3.88 (dd, J = 9.8, 5.9 Hz, 2H), 3.63 (d, J = 9.3 Hz, 1 H), 3.50 (m, 3H), 3.28 (m, 2H), 3.10 (m, 1 H), 2.78 (m, 4H), 2.45 (s, 3H), 2.27 (s, 3H), 1.60 (m, 6H) . m/z (ES+) : 548 [M + H] ⁺ .

Exa mple 78 : Compound 78

( lS,8aS)-7,7-bis(2-hvdroxyethyl)-/V-(3-methoxy-5-(trifluoromethyl)benzyl)-/V-methyl-6-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 58 ( 100 mg , 0.18 mmol) in DCM ( 10 ml_) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ ( 137 mg, 3.6 mmol) . The reaction mixture was allowed to wa rm to room temperature and stirred for 20 h . After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum . The residue was purified by Prep-HPLC to give the compound 78 (40 mg , yield: 39.5%). *H NMR (400 MHz, DMSO) δ ppm 7.40 (m, 1H), 7.10 (dd, J = 7.4, 4.8 Hz, 4H), 6.82 (d, J = 17.5 Hz, 2H), 4.41 (m, 4H), 3.88 (t, J = 11.9 Hz, 2H), 3.70 (m, 4H), 3.50(m, 4H), 3.25 (m, 1H), 3.13 (t, J = 10.3 Hz, 1H), 2.81 (m, 4H), 2.44 (s, 3H), 1.52 (m, 6H). m/z (ES+): 564 [M + H] ⁺ .

Example 79: Compound 79

(lS,8aS^')-/V-(3-chloro-5-(tnfluoromethyl^')benzyl^')-7,7-bis(2-hvdroxyethyl^')-/V-methyl-6-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 58 (100 mg , 0.18 mmol) in DCM (10 ml_) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (137 mg, 3.6 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 79 (15 mg , yield: 15%). H NMR (400 MHz, CDCI₃) δ ppm 7.47 (s, 1H), 7.28 (s, 2H), 7.21 (s, 3H), 7.11 (s, 1H), 7.00 (s, 1H), 4.62 (d, J = 15.2 Hz, 1H), 4.30 (m, 1H), 4.16 (m, 1H), 4.07 (m, 1H), 3.76 (m, 4H), 3.62 (m, 1H), 3.40 (m, 1H), 3.17 (m, 1H), 3.02 (m, 1H), 2.99 (s, 3H), 2.52 (s, 3H), 1.85 (m, 6H). m/z (ES+): 568 [M + H] ⁺ .

Example 80: Compound 80

riS,8aS^')-7,7-bisr2-hvdroxyethvn-/V-methyl-6-oxo-l-o-tolyl-/V-r3-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 58 (90 mg , 0.17 mmol) in DCM (10 ml_) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (194 mg, 5.1 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 80 (10 mg , yield: 11%). *H NMR (400 MHz, CDCI₃) δ ppm 7.48 (d, J = 7.6 Hz, IH), 7.30 (m, 2H), 7.21 (m, 4H), 6.88 (d, J = 8.0 Hz, IH), 4.62 (d, J = 15.2 Hz, IH), 4.35 (m, IH), 4.10(m, 2H), 3.78 (m, 4H), 3.62 (m, IH), 3.30 (m, IH), 3.15 (m, 2H), 2.96 (m, IH), 2.92 (s, 3H),2.56 (s, 3H), 2.28 (s, IH), 1.85 (m, 6H). m/z (ES+): 534 [M + H] ⁺ .

Example 81 & Example 82: Compound 81 & Compound 82

(lS,8aS)-/V-(l-(3,5-bis(trifluoromethyl)phenyl)-3-hydroxypropyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 64 (30 mg , 0.05 mmol) in DCM (10 ml_) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (53 mg, 1.4 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 81 (4 mg, yield: 11%) and the compound 82 (4 mg, yield: 11%).

JH NMR (400 MHz, CDCI₃) δ ppm 7.83 (s, IH), 7.63 (s, 2H), 7.40 (m, IH), 7.20 (m, IH), 5.58 (dd, J = 15.2, 2.8 Hz, IH), 4.15 (m, 2H), 4.12 (m, IH), 3.83 (m, 3H), 3.64 (m, IH), 3.31 (m, 2H), 3.14 (m, IH), 3.06 (m, 3H), 2.68 (s, 3H),2.56 (s, 3H), 2.47 (m, IH), 2.21 (m, 6H), 1.90 (m, 6H). m/z (ES+): 646 [M + H] ⁺ .

^JH NMR (400 MHz, CDCI₃) δ ppm 7.80 (s, IH), 7.41 (m, 2H), 7.28 (s, IH), 7.21 (m, IH), 7.15 (m, 3H), 6.88 (dd, J = 11.2, 2.4 Hz, IH), 4.16 (m, 2H), 4.07 (m, 6H), 3.83 (m, 2H), 3.14 (m, IH), 3.03 (m, 2H), 2.15 (s, 3H), 2.00 (m, 10H). m/z (ES+): 646 [M + H] ⁺ . Exa mple 83 : Compound 83

i lS,8aSV/V-i l-i3 ,5-bisitrifluoromethvnphenvnpropylV7,7-bisi2-hvdroxyethvn-/V-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 67 (50 mg, 0.08 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (61 mg, 1.6 mmol) . The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum . The residue was purified by Prep-HPLC to give the compound 83 ( 12 mg, yield : 23.8%) . *H NMR (400 MHz, CDCI₃) δ ppm 7.72 (s, 1 H), 7.37 (s, 2H), 7.18 (m, 3H), 7.10 (dd, J = 9.7, 4.2 Hz, 1H), 5.36 (dd, J = 10.9, 4.9 Hz, 1 H), 4.12 (dd, J = 28.4, 11.2 Hz, 2H), 3.93 (m, 2H), 3.76 (m, 2H), 3.64 (m, 1H), 3.39 (d, J = 10.8 Hz, 1 H), 3. 17 (td, J = 12.5, 3.6 Hz, 1H), 2.98 (td, J = 12.0, 3.2 Hz, 1 H), 2.81 (s, 3H), 2.54 (d, J = 7.8 Hz, 3H), 2.06 (m, 1H), 1.92 (dd, J = 12.2, 6.1 Hz, 2H), 1.90 (m, 4H), 1.78 (m, 3H), 0.97 (t, J = 7.2 Hz, 3H) . m/z (ES+) : 630 [M + H] ⁺ .

Exa mple 84 : Compound 84

f lS.8aSV7.7-bisf2-hvdroxyethvn-yv-methyl-yy-ffSV l-f3-methyl-5-

(trifluoromethyl)phenyl)ethyl)-6-oxo- l-o-tolylhexahvdropyrrolor i ,2-a1 pyrazine-2( l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 81 ( 100 mg, 0.18 mmol) in DCM (30 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ ( 137 mg, 3.6 mmol) . The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 84 (12 mg, yield: 23.8%). *H NMR (400 MHz, CDCI₃) δ ppm 7.32 (m, 2H), 7.22 (m, 3H), 7.05 (s, 1H), 6.73 (s, 1H), 5.53 (d, J = 7.1 Hz, 1H), 4.10 (dd, J = 25.2, 11.1 Hz, 2H), 3.89 (m, 1H), 3.76 (qd, J = 11.4, 5.4 Hz, 3H), 3.64 (m, 1H), 3.33 (d, J = 10.8 Hz, 1H), 3.14 (td, J = 12.6, 3.6 Hz, 1H), 2.95 (td, J = 12.1, 3.2 Hz, 1H), 2.77 (s, 3H), 2.55 (d, J = 10.5 Hz, 3H), 2.25 (s, 3H), 1.92 (t, J = 5.9 Hz, 2H), 1.89 (m, 3H), 1.78 (m, 3H), 1.46 (d, J = 7.1 Hz, 3H). m/z (ES+): 562 [M + H] ⁺ .

Example 85: Compound 85

flS.8aSV7.7-bisf2-hvdroxyethvn-yv-methyl-yy-ffRVl-f3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 77 (100 mg, 0.18 mmol) in DCM (30 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (137 mg, 3.6 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 85 (10 mg, yield: 20%). *H NMR (400 MHz, CDCI₃) δ ppm 7.33 (s, 1H), 7.28 (m, 1H), 7.20 (m, 3H), 7.14 (m, 1H), 7.00 (s, 1H), 5.49 (d, J = 7.8 Hz, 1H), 4.10 (m, 2H), 3.82 (m, 4H), 3.59 (m, 1H), 3.33 (m, 1H), 3.15 (m, 1H), 3.00 (m, 1H), 2.64 (s, 3H), 2.56 (s, 3H), 2.35 (s, 3H), 1.76 (m, 8H), 1.40 (m, 3H). m/z (ES+): 562 [M + H] ⁺ .

Example 86: Compound 86

flS.8aSVyv-ffSVl-f3.5-bisftrifluoromethvnphenvn-2-hvdroxyethvn-7.7-bisf2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 87 (100 mg, 0.16 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (62 mg, 1.6 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 86 (20 mg, yield: 51%). *H NMR (400 MHz, CDCI₃) δ ppm 7.71 (s, 1H), 7.31 (s, 2H), 7.26 (s, 1H), 7.15 (s, 2H), 5.37 (q, 1H), 4.06 (m, 3H), 3.71 (m, 5H), 3.47 (m, 3H), 3.15 (m, 2H), 2.93 (s, 3H), 2.52 (s, 4H), 1.93 (m, 1H), 1.77 (m, 6H). m/z (ES+): 632 [M + H] ⁺ .

Example 87: Compound 87

ilS,8aS)-/V-iiR)-l-i3,5-bisitrifluoromethvnphenvn-2-hvdroxyethvn-7,7-bisi2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(lH)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 90 (70 mg, 0.11 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (125 mg, 3.3 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the compound 87 (20 mg, yield: 51%). *H NMR (400 MHz, CDCI₃) δ ppm 7.79 (s, 1H), 7.51 (s, 2H), 7.26 (m, 1H), 7.18 (m, 2H), 7.15 (m, 1H), 5.22 (m, 1H), 4.10 (m, 3H), 3.97 (m, 2H), 3.87 (m, 2H), 3.60 (m, 4H), 3.20 (m, 3H), 2.70 (s, 3H), 2.65 (m, 1H), 2.52 (s, 3H), 1.88 (m, 4H) . m/z (ES+) : 632 [M + H] ⁺ .

Exa mple 88 : Compound 88

riS,8aS^')-7,7-bisr2-hvdroxyethvn-/V-methyl-6-oxo- l-o-tolyl-/V-rrR^')- l-r3-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 91 (82 mg, 0.15 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (60 mg, 1.5 mmol) . The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound (33 mg, yield : 40%) . H NMR (400 MHz, CDCI₃) δ ppm 7.54 (d, J = 7.7 Hz, 1 H), 7.45 (m, 2H), 7.28 (m, 5H), 5.52 (d, J = 6.8 Hz, 1H), 4.10 (t, J = 12.4 Hz, 2H), 3.79 (dtt, J = 28.9, 11.4, 5.8 Hz, 4H), 3.65 (m, 1H), 3.32 (d, J = 11.7 Hz, 1 H), 3.15 (t, J = 12.3 Hz, 1 H), 3.00 (dd, J = 11.8, 9.0 Hz, 1 H), 2.67 (s, 3H), 2.57 (s, 3H), 1.92 (t, J = 5.8 Hz, 2H), 1.88 (m, 2H), 1.71 (s, 4H), 1.38 (d, J = 6.7 Hz, 3H) ; m/z (ES+) : 548 [M + H] ⁺ .

Exa mple 89 : Compound 89

riS,8aS^')-/V-rrR^')- l-r3-chloro-5-rtrifluoromethvnphenvnethvn-7,7-bisr2-hvdroxyethvn- -methyl-6-oxo- l-o-tolylhexa hvdropyrrolor i ,2-a1 pyrazine-2( l/-/)-carboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 95 (65 mg, 0.11 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (44 mg, 1.1 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (16.4 mg, yield: 25%). *H NMR (400 MHz, CDCI₃) δ ppm 7.52 (s, 1H), 7.26 (s, 2H), 7.23 (s, 1H), 7.19 (dd, J = 3.9, 2.0 Hz, 2H), 7.18 (m, 1H), 5.49 (q, J = 6.8 Hz, 1H), 4.10 (dd, J = 18.9, 11.3 Hz, 2H), 3.80 (ddt, J = 23.3, 11.3, 6.0 Hz, 4H), 3.64 (m, 1H), 3.32 (d, J = 11.9 Hz, 1H), 3.18 (m, 1H), 3.04 (m, 1H), 2.68 (s, 3H), 2.55 (s, 3H), 1.91 (t, J = 5.7 Hz, 2H), 1.83 (dd, J = 6.2, 3.9 Hz, 3H), 1.75 (m, 2H), 1.38 (d, J = 6.9 Hz, 3H); m/z (ES+): 582 [M+H] ⁺ .

Example 90: Compound 90

riS,8aSV/V-rrSVl-r3-chloro-5-rtrifluoromethvnphenvnethvn-7,7-bisr2-hvdroxyethvn-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 96 (50 mg, 0.088 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (67 mg, 1.75 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (10 mg, yield: 20%). H NMR (400 MHz, CDCI₃) δ ppm 7.45 (s, 1H), 7.26 (d, J = 3.5 Hz, 1H), 7.20 (d, J = 2.8 Hz, 3H), 7.08 (s, 1H), 6.94 (s, 1H), 5.52 (q, J = 7.0 Hz, 1H), 4.19 (m, 1H), 4.06 (d, J = 9.7 Hz, 1H), 3.90 (m, 1H), 3.74 (ddd, J = 16.3,

10.8, 5.8 Hz, 3H), 3.64 (m, 1H), 3.33 (d, J = 11.5 Hz, 1H), 3.15 (td, J = 12.5, 3.3 Hz, 1H), 2.95 (td, J = 12.0, 2.9 Hz, 1H), 2.81 (s, 3H), 2.55 (s, 3H), 1.92 (t, J = 6.1 Hz, 2H), 1.85 (dd, J = 13.4, 7.3 Hz, 2H), 1.74 (ddd, J = 26.5, 13.8, 7.1 Hz, 2H), 1.47 (d, J = 7.1 Hz, 3H), 1.27 (m, J = 8.5, 5.7 Hz, 1H); m/z (ES+): 582 [M + H] ⁺ .

Example 91: Compound 91 riS.8aSV7.7-bisr2-hvdroxyethvn-/V-rrRVl-r3-methoxy-5- (trifluoromethvnphenvnethvn-/V-methyl-6-oxo-l-o-tolylhexahvdropyrrolor i,2-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 100 ( 100 mg, 0.18 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ ( 137 mg, 3.6 mmol) . The reaction mixture was allowed to wa rm to room tempraure and stirred for 20 h . After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound ( 10 mg, yield : 9.6%) . *H NMR (400 MHz, CDCI₃) δ ppm 7.27 (d, J = 6.9 Hz, 1 H), 7.23 (m, 3H), 7.00 (d, J = 18.1 Hz, 2H), 6.81 (s, 1 H), 5.47 (q, J = 6.8 Hz, 1 H), 4.09 (dd, J = 16.7, 11.4 Hz, 2H), 3.91 (m, 7H), 3.60 (dt, J = 11.8, 6.0 Hz, 1 H), 3.43 (m, 4H), 2.68 (s, 3H), 2.56 (s, 4H), 1.98 (m, 6H), 1.32 (t, J = 13.3 Hz, 3H) ; m/z (ES+) : 578 [M + H] ⁺ .

Exa mple 92 : Compound 92

i lS,8aS)-/V-iiS)- l-i3-fluoro-5-itrifluoromethvnphenvnethvn-7,7-bisi2-hvdroxyethvn-/V-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 103 (70 mg, 0.126 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (96 mg, 2.52 mmol) . The reaction mixture was allowed to wa rm to room tempraure and stirred for 20 h . After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (20 mg, yield: 28%). *H NMR (400 MHz, CDCI₃) δ ppm 7.29 (s, 1H), 7.20 (s, 2H), 7.20 (m, 2H), 7.03 (s, 1H), 6.55 (d, J = 9.4 Hz, 1H), 5.52 (q, J = 7.0 Hz, 1H), 4.15 (d, J = 12.7 Hz, 1H), 4.07 (d, J = 9.7 Hz, 1H), 3.87 (dd, J = 11.6, 5.9 Hz, 1H), 3.83 (m, 3H), 3.66 (m, 1H), 3.33 (d, J = 11.8 Hz, 1H), 3.16 (t, J = 12.4 Hz, 1H), 2.96 (dd, J = 12.1, 9.4 Hz, 1H), 2.82 (s, 3H), 2.55 (s, 3H), 1.93 (t, J = 5.8 Hz, 2H), 1.90 (m, 3H), 1.80 (m, 3H), 1.48 (d, J = 7.1 Hz, 3H); m/z (ES+): 566 [M + H] ⁺ .

Example 93: Compound 93

riS,8aS)-/V-iiR)-l-i3-fluoro-5-itrifluoromethvnphenvnethvn-7,7-bisi2-hvdroxyethvn-/V-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 104 (65 mg, 0.11 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (44 mg, 1.1 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (20 mg, yield: 28%). *H NMR (400 MHz, CDCI₃) δ ppm 7.29 (s, 1H), 7.25 (t, J = 9.2 Hz, 2H), 7.20 (m, 2H), 7.14 (dd, J = 9.4, 3.6 Hz, 1H), 6.94 (d, J = 9.4 Hz, 1H), 5.61 (m, 1H), 4.10 (dd, J = 19.0, 11.3 Hz, 2H), 3.86 (m, 4H), 3.64 (m, 1H), 3.32 (d, J = 11.8 Hz, 1H), 3.18 (m, 1H), 3.02 (td, J = 11.9, 3.1 Hz, 1H), 2.69 (s, 3H), 2.56 (s, 3H), 1.92 (d, J = 5.8 Hz, 2H), 1.84 (dd, J = 12.6, 5.6 Hz, 3H), 1.75 (m, 3H), 1.38 (d, J = 6.9 Hz, 3H); m/z (ES+): 566 [M + H] ⁺ .

Example 94: Compound 94

flS.8aSVyv-ffSVl-f3-fluoro-5-ftrifluoromethvnphenvn-2-hvdroxyethvn-7.7-bisf2- hvdroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 105 (65 mg, 0.11 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (44 mg, 1.1 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (28.8 mg, yield: 35%). *H NMR (400 MHz, CDCI₃) δ ppm 7.29 (s, 2H), 7.19 (t, J = 7.6 Hz, 4H), 6.96 (s, 1H), 6.63 (d, J = 9.1 Hz, 1H), 5.37 (s, 1H), 4.13 (s, 1H), 4.11 (s, 1H), 3.94 (m, 1H), 3.84 (m, 3H), 3.61 (s, 1H), 3.48 (d, J = 12.1 Hz, 1H), 3.16 (d, J = 11.5 Hz, 1H), 2.94 (s, 3H), 2.55 (s, 3H), 1.95 (s, 1H), 1.85 (d, J = 4.6 Hz, 3H), 1.84 (s, 4H), 1.73 (d, J = 13.9 Hz, 1H), 1.28 (s, 1H); m/z (ES+): 582 [M + H] ⁺ . Example 95: Compound 95

ilS,8aS)-/V-iiS)-2-hvdroxy-l-i3-methoxy-5-itrifluoromethvnphenvnethvn-7,7-bisi2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 109 (60 mg, 0.103 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (78 mg, 2.06 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (20 mg, yield: 32.7%). ^JH NMR (400 MHz, CDCI₃) δ ppm 7.30 (d, J = 7.0 Hz, 1H), 7.16 (d, J = 2.9 Hz, 3H), 6.96 (s, 1H), 6.73 (d, J = 12.6 Hz, 1H), 6.59 (s, 1H), 5.33 (dd, J = 10.0, 4.9 Hz, 1H), 4.10 (dd, J = 17.0, 7.1 Hz, 3H), 3.85 (dd, J = 20.8, 9.4 Hz, 2H), 3.81 (m, 4H), 3.66 (s, 3H), 3.62 (m, 3H), 3.16 (t, J = 10.8 Hz, 1H), 2.95 (d, J = 12.2 Hz, 1H), 2.91 (s, 3H), 2.54 (s, 3H), 1.96 (dd, J = 13.4, 4.8 Hz, 1H), 1.94 (m, 5H), 1.75 (m, 1H); m/z (ES+): 594 [M + H] ⁺ .

Example 96: Compound 96

ilS,8aSV/V-iiSV2-hvdroxy-l-i3-itrifluoromethvnphenvnethylV7,7-bisi2-hvdroxyethvn- -methyl-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/^')-carboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 114 (50 mg, 0.09 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (70 mg, 1.8 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (10 mg, yield: 20%). *H NMR (400 MHz, DMSO) δ ppm 7.54 (d, J = 7.8 Hz, 1H), 7.36 (dd, J = 9.9, 5.1 Hz, 2H), 7.22 (s, 1H), 7.12 (t, J = 5.7 Hz, 3H), 6.99 (d, J = 7.6 Hz, 1H), 5.20 - 5.11 (m, 1H), 5.02 (t, J = 5.3 Hz, 1H), 4.50 (t, J = 5.0 Hz, 1H), 4.37 (t, J = 5.1 Hz, 1H), 3.95 (dt, J = 11.3, 5.6 Hz, 1H), 3.87 (dd, J = 16.7, 11.4 Hz, 2H), 3.77 - 3.68 (m, 1H), 3.63 (dd, J = 16.9, 7.8 Hz, 1H), 3.48 (dd, J = 19.0, 10.2 Hz, 3H), 3.32 (s, 2H), 3.12 (t, J = 10.5 Hz, 1H), 2.86 (s, 3H), 2.68 (t, J = 10.5 Hz, 1H), 2.43 (s, 3H), 1.70 (dd, J = 15.0, 7.3 Hz, 2H), 1.50 (dt, J = 20.3, 10.3 Hz, 2H), 1.24 (s, 1H), 0.93 - 0.83 (m, 1H); m/z (ES+): 564 [M + H] ⁺ .

Example 111: Compound 111

ilS,8aS)-/V-iiS)-2-hvdroxy-l-i3-methyl-5-itrifluoromethvnphenvnethvn-7,7-bisi2- hvdroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 117 (74 mg, 0.11 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (70 mg, 1.8 mmol) . The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound ( 17 mg, yield : 23%) . *H NMR (400 MHz, CDCI₃) δ ppm 7.30 (dd, J = 15.0, 3.9 Hz, 3H), 7.18 (d, J = 9.7 Hz, 3H), 6.95 (s, 1 H), 6.74 (s, 1 H), 5.36 (dd, J = 9.9, 4.8 Hz, 1 H), 4. 13 (t, J = 10.2 Hz, 3H), 3.93 (m, 2H), 3.76 (dd, J = 15.1, 10.3 Hz, 3H), 3.65 (m, 1 H), 3.48 (d, J = 11.8 Hz, 1 H), 3.15 (d, J = 12.3 Hz, 1 H), 2.95 (d, J = 12.3 Hz, 1 H), 2.91 (s, 3H), 2.56 (s, 3H), 2.27 (s, 3H), 2.01 (m, 2H), 1.86 (m, 4H), 1.77 (m, 1 H), 1.27 (s, 1 H); m/z (ES+) : 578 [M + H] ⁺ .

Exa mple 97 : Compound 97

riS,8aS^')-/V-rrR^')- l-r3-rdifluoromethvn-5-rtrifluoromethvnphenvnethvn-7,7-bisr2- hvdroxyethyl)-/V-methyl-6-oxo- l-o-tolylhexa hvdropyrrolor i ,2-a1 pyrazine-2( l/-/)- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 125 (70 mg, 0.12 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (44 mg, 1.1 mmol) . The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM . The orga nic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound ( 14 mg, yield : 20%) . H NMR (400 MHz, CDCI₃) δ ppm 7.67 (d, J = 12.9 Hz, 1 H), 7.48 (s, 1 H), 7.35 (s, 1 H), 7.25 (dd, J = 20.3, 12.9 Hz, 2H), 7.22 (m, 2H), 7.17 (m, 1H), 6.59 (t, J = 55.9 Hz, 1H), 5.53 (q, J = 6.8 Hz, 1H), 4.10 (t, J = 10.4 Hz, 2H), 3.89 (m, 4H), 3.64 (m, 1H), 3.32 (d, J = 11.8 Hz, 1H), 3.15 (td, J = 12.3, 3.2 Hz, 1H), 3.02 (dd, J = 11.8, 9.0 Hz, 1H), 2.68 (s, 3H), 2.55 (s, 3H), 1.97 (m, 3H), 1.83 (dd, J = 13.3, 6.3 Hz, 2H), 1.76 (m, 2H), 1.42 (d, J = 6.8 Hz, 3H); m/z (ES+): 598 [M + H] ⁺ .

Example 98: Compound 98

riS,8aS^')-/V-rrR^')-l-r3-rdifluoromethvn-5-rtnfluoromethvnphenvnethvn-7,7-bisr2- hvdroxyethyl^')-/V-methyl-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/^')- ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 130 (80 mg, 0.14 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (44 mg, 1.1 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (14 mg, yield: 18%). H NMR (400 MHz, CDCI3) δ ppm 7.47 (s, 1H), 7.28 (s, 2H), 7.20 (s, 2H), 7.02 (d, J = 17.5 Hz, 1H), 6.98 (s, 1H), 5.43 (m, 1H), 4.17 (m, 2H), 3.94 (m, 4H), 3.61 (s, 1H), 3.48 (d, J = 11.8 Hz, 1H), 3.17 (t, J = 10.9 Hz, 1H), 2.97

(d, J = 9.8 Hz, 1H), 2.95 (s, 3H), 2.55 (s, 3H), 2.05 (m, 1H), 1.82 (dd, J = 19.9, 7.1 Hz, 4H), 1.75 (s, 4H), 1.29 (s, 2H); m/z (ES+): 598 [M + H] ⁺ .

Example 99: Compound 99

riS,8aSV/V-rrSVl-r3,5-bisrtrifluoromethvnphenvnethvn-7,7-bisr2-hvdroxyethvn methyl-6-oxo-l-o-toly I hexahyd ropy rrolo[l,2-alpyrazine-2(l/-/)-ca rboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 135 (40 mg, 0.066 mmol) in DCM (10 mL) at -78°C until a pale blue colour persisted. The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (76 mg, 1.98 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (14 mg, yield: 35%). *H NMR (400 MHz, CDCI₃) δ ppm 7.73 (s, 1H), 7.36 (s, 2H), 7.28 (s, 1H), 7.25 (m, 1H), 7.17 (m, 2H), 5.60 (q, J = 7.2 Hz, 1H), 4.17 (m, 2H), 3.87 (m, 4H), 3.61 (m, 1H), 3.37 (d, J = 11.6 Hz, 1H), 3.19 (m, 2H), 3.00 (m, 1H), 2.82 (s, 3H), 2.54 (s, 3H), 2.32 (m, 1H), 1.87 (m, 6H), 1.29 (m, 3H); m/z (ES+): 616 [M + H] ⁺ .

Example 100: Compound 100

ri'S,8a'S^')-/V-rrR^')-l-r3,5-bisrtrifluoromethvnphenvnethvn-/V-methyl-6'-oxo-l'-o- tolyloctahydro-l'/-/-spiro[pyran-4,7'-pyrrolo[l,2-alpyrazinel-2'(6'/-/)-carboxamide

To a solution of (lS,8aS)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(l/-/)- carboxamide (70 mg, 0.11 mmol) in 5 mL of DCM, was added MsCI (38 mg, 0.33 mmol) at 0 °C. The mixture was stirred for 1.5 h, and concentrated in high vacuum. The residue was treated with mixture of H₂0 (5 mL) and TEA (0.5 mL) and then heated to 65 °C untill the reaction was completed. The reaction mixture was extracted with DCM (2 x 15 mL) and the organic layers were dried over anhydrous Na₂S0₄and then concentrated in high vaccum. The residue was purified by Prep-HPLC to give the title compound (15 mg, yield: 23%). H NMR (400 MHz, CDCI₃) δ ppm 7.71 (s, 1H), 7.46 (s, 2H), 7.22 (m, 4H), 5.47 (d, J = 7.0 Hz, 1H), 4.08 (d, J = 12.8 Hz, 1H), 3.95 (d, J = 9.7 Hz, 2H), 3.81 (dd, J = 7.6, 4.0 Hz, 1H), 3.65 (d, J = 9.1 Hz, 1H), 3.36 (dd, J = 13.4, 6.3 Hz, 2H), 3.20 (d, J = 11.6 Hz, 1H), 3.05 (td, J = 12.3, 3.4 Hz, 1H), 2.91 (dt, J = 11.8, 5.9 Hz, 1H), 2.63 (s, 3H), 2.46 (s, 3H), 2.11 (dd, J = 17.6, 6.9 Hz, 1H), 1.89 (dd, J = 13.1, 7.2 Hz, 1H), 1.79 (dd, J = 17.0, 7.0 Hz, 1H), 1.49 (s, 2H), 1.31 (t, J = 8.1 Hz, 6H), 1.18 (s, 3H), 0.86 (s, 2H); m/z (ES+): 598 [M + H] ⁺ . Example 101: Compound 101

fl'S.8a'SVA-ffRVl-f3.5-bisftrifluoromethvnphenvnethvn-yv-methyl-6'-oxo-l'-o-

To a solution of (lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-/V-((R)-l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(l/-/)- carboxamide (56 mg, 0.1 mmol) in 5 mL of DCM, was added MsCI (38 mg, 0.33 mmol) at 0 °C. The mixture was stirred for 1.5 h, and concentrated in high vacuum. The residue was treated with mixture of H₂0 (5 mL) and TEA (0.5 mL) and then heated to 65 °C untill the reaction was completed. The reaction mixture was extracted with DCM (2 x 15 mL) and the organic layers were dried over anhydrous Na₂S0₄and then concentrated in high vaccum. The residue was purified by Prep-HPLC to give the title compound (16 mg, yield: 29%). *H NMR (400 MHz, CDCI₃) δ ppm 7.31 (s, IH), 7.26 (s, IH), 7.20 (m, 4H), 6.99 (s, IH), 5.47 (d, J = 7.2 Hz, IH), 4.14 (d, J = 13.2 Hz, IH),

4.02 (m, 2H), 3.69 (q, J = 8.0 Hz, IH), 3.45 (m, IH), 3.38 (m, IH), 3.12 (m, IH), 2.98 (m, IH), 2.63 (s, 3H), 2.54 (s, 3H), 2.33 (s, 3H),2.21 (m, IH), 1.89 (m, 2H), 1.49 (m, 7H); m/z (ES+): 544 [M + H] ⁺ . Example 102 & 103: Compound 102 & 103

riS,8aSV7-rhvdroxymethvn-/V-methyl-/V-rrR')-l-r3-methyl-5-

(trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/)- ca rboxamide

ilS,8aS)-7,7-bisihvdroxymethvn-/V-methyl-/V-iiR)-l-i3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahvdropyrrolori,2-a1pyrazine-2(l/-/)- ca rboxamide

To a solution of Intermediate 136 (200 mg, 0.375 mmol) in THF (4 ml_) at 0 °C was added LiBH₄(16 mg, 0.75 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 2 h. After quenched with water, the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give mono-hydroxymethyl substituted compound 102 (15 mg, yield: 8%) and bis- hydroxymethyl substituted compound 103 (8 mg, yield: 4%).

Compound 102: ^JH NMR (400 MHz, CDCI₃) δ ppm 7.24 (s, 1H), 7.21 (m, 1H), 7.09 (d, J = 5.8 Hz, 3H), 7.07 (m, 1H), 6.92 (s, 1H), 5.40 (q, J = 6.8 Hz, 1H), 4.11 (m, 2H), 3.81 (dt, J = 12.0, 6.0 Hz, 1H), 3.64 (dt, J = 15.4, 7.7 Hz, 2H), 3.21 (t, J = 16.7 Hz, 1H), 3.06 (t, J = 12.3 Hz, 1H), 2.91 (td, J = 11.8, 3.0 Hz, 1H), 2.55 (s, 3H), 2.51 (d, J = 9.8 Hz, 1H), 2.47 (s, 3H), 2.26 (s, 3H), 1.85 (ddd, J = 12.8, 9.0, 7.0 Hz, 1H), 1.50 (m, 1H), 1.29 (d, J = 6.4 Hz, 3H); m/z (ES+): 504 [M + H] ⁺ .

Compound 103: H NMR (400 MHz, CDCI₃) δ ppm 7.24 (s, 1H), 7.17 (s, 1H), 7.10 (s, 2H), 7.09 (m, 2H), 6.92 (s, 1H), 5.41 (d, J = 7.0 Hz, 1H), 4.06 (t, J = 12.0 Hz, 2H), 3.83 - 3.69 (m, 2H), 3.68 (m, 3H), 3.22 (d, J = 12.0 Hz, 1H), 3.09 (dd, J = 20.2, 7.9 Hz, 1H), 2.90 (dd, J = 11.9, 8.8 Hz, 1H), 2.73 (s, 1H), 2.56 (s, 3H), 2.48 (d, J = 14.3 Hz, 3H), 2.26 (s, 3H), 2.22 (m, 1H), 1.75 (dd, J = 13.6, 7.9 Hz, 1H), 1.60 (m, 1H), 1.29 (d, J = 6.3 Hz, 3H); m/z (ES+): 534 [M + H] ⁺ .

Example 104: Compound 104

riS,8aS^')-/V-rrR^')-l-r3,5-bisrtrifluoromethvnphenvnethvn-7,7-bisrhvdroxymethvn-/V-

To a solution of Intermediate 137 (166 mg, 0.26 mmol) in MeOH (5 ml_) at 0 °C was added LiBH₄(ll mg, 0.52 mmol). The reaction mixture was allowed to warm to room tempraure and stirred for 2 h. After quenched with water, the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (6 mg, yield: 3.9%). *H NMR (400 MHz, CDCI₃) δ ppm 7.70 (s, 3H), 7.47 (s, 6H), 7.19 (m, 13H), 5.47 (d, J = 6.8 Hz, 3H), 4.06 (dd, J = 20.7, 11.4 Hz, 6H), 3.92 (m, 15H), 3.30 (m, 10H), 2.65 (d, J = 24.4 Hz, 11H), 2.46 (d, J = 14.0 Hz, 9H), 2.15 (s, 3H), 1.77 (dd, J = 13.5, 7.9 Hz, 4H), 1.62 (m, 3H), 1.32 (d, J = 6.9 Hz, 10H); m/z (ES+): 588 [M + H] ⁺ .

Example 105: Compound 105

ri'S.Sa'SV/V-rrRVl-rS.S-bisrtrifluoromethvnphenvnethvn-A/.l-dimethyl-e'-oxo-l'-o- tolyltetrahydro-l'/-/-spiro[piperidine-4,7'-pyrrolo[l,2-alpyrazinel-2'(6'/-/)-carboxamide, formic acid salt

To a solution of (lS,8aS)-N-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-N-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(lH)- carboxamide (70 mg, 0.11 mmol) in DCM (5 mL), was added MsCI (38 mg, 0.33 mmol) at 0 °C. The mixture was stirred for 1.5 h, and concentrated in high vacuum. The residue was treated with mixture of methanamine hydrochloride (10 mg, 0.15 mmol) in TEA (0.5 mL) and then heated to 65 °C untill the reaction was completed. The reaction mixture was extracted with DCM (2 x 15 mL) and the organic layers were dried over anhydrous Na₂S0₄and then concentrated in high vaccum. The residue was purified by Prep-HPLC to give the title compound (13 mg, yield: 20%). H NMR (400 MHz, CDCI₃) δ ppm 7.79 (s, 1H), 7.55 (s, 2H), 7.28 (s, 1H), 7.19 (ddd, J = 19.6, 11.8, 7.5 Hz, 4H),

5.56 (d, J = 6.9 Hz, 1H), 4.11 (d, J = 12.9 Hz, 1H), 4.03 (d, J = 9.8 Hz, 1H), 3.76 (d, J = 8.1 Hz, 2H), 3.39 (m, 2H), 3.20 (m, 2H), 2.99 (t, J = 10.6 Hz, 1H), 2.72 (s, 6H), 2.52 (s, 3H), 2.24 (s, 1H), 2.06 (d, J = 14.9 Hz, 2H), 1.87 (d, J = 12.8 Hz, 1H), 1.84 (m, 1H), 1.60 (dd,_7 = 13.5, 7.9 Hz, 1H), 1.40 (d, J = 6.9 Hz, 3H); m/z (ES+): 611 [M- HCOOH + H] ⁺ .

Example 106: Compound 106 fl'S,8a'SV/V-ffRVl-f3,5-bisftnfluorome^

tolyltetrahvdro- /^-spirorpipendine-4,7'-py^

formic acid salt

To a solution of (lS,8aS)-N-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-N-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(lH)- carboxamide (70 mg, 0.11 mmol) in DCM (5 mL), was added MsCI (38 mg, 0.33 mmol) at 0 °C. The mixture was stirred for 1.5 h, and concentrated in high vacuum. The residue was treated with NH40H (19 mg, 0.15 mmol) and then heated to 65 °C untill the reaction was completed. The reaction mixture was extracted with DCM (2 x 20 mL) and the organic layers were dried over anhydrous Na₂S0₄and then concentrated in high vaccum. The residue was purified by Prep-HPLC to give the title compound (13 mg, yield: 20%). ^ NMR (400 MHz, CD₃OD) δ ppm 8.51 (s, 1H), 7.87 (s, 1H), 7.67 (s, 2H), 7.35 (d, J = 7.3 Hz, 1H), 7.19 (m, 3H), 5.44 (d, J = 6.8 Hz, 1H), 4.15 (d, J = 10.0 Hz, 1H), 4.05 (m, 2H), 3.54 (dd, J = 23.4, 8.7 Hz, 2H), 3.10 (m, 3H), 2.76 (s, 3H), 2.51 (s, 3H), 2.23 (m, 1H), 1.91 (dd, J = 13.1, 5.4 Hz, 1H), 1.74 (m, 3H), 1.50 (d, J = 7.0 Hz, 3H), 1.29 (s, 3H), 0.95 (dt, J = 14.7, 7.3 Hz, 1H); m/z (ES+): 597 [M-HCOOH +H] ⁺ .

Example 107: Compound 107

riS,8aS^')-/V-methyl-/V-rrR^')-l-r3-methyl-5-rtrifluoromethvnphenvnethvn-6-oxo-l-o-

To a solution of triphosgene (254 mg, 0.87 mmol) in EtOAc (5 mL) at 0 °C was added solution of (lS,8aS)-l-o-tolylhexahydropyrrolo[l,2-a]pyrazin-6(7H)-one (400 mg, 1.73 mmol), DMAP (21 mg, 0.173 mmol) and TEA (524 mg, 5.19 mmol in EtOAc (5 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-N-methyl-l-(3-methyl-5- (trifluoromethyl)phenyl)ethanamine (563 mg, 2.6 mmol) in EtOAc (2 mL) and TEA (524 mg, 5.19 mmol). The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel chromatography (DCM/MeOH = 20/l to

10/1) to give the title compound (350 mg, yield: 85%). *H NMR (400 MHz, CDCI₃) δ ppm 7.32 (s, 1H), 7.25 (d, J = 8.0 Hz, 1H), 7.19 (d, J = 7.4 Hz, 2H), 7.14 (ddd, J = 17.5, 10.0, 4.2 Hz, 2H), 7.00 (s, 1H), 5.48 (q, J = 6.9 Hz, 1H), 4.22 (m, 2H), 3.71 (dd, J = 17.0, 7.3 Hz, 1H), 3.29 (d, J = 11.8 Hz, 1H), 3.11 (td, J = 12.4, 2.7 Hz, 1H), 2.95 (td, J = 11.9, 3.2 Hz, 1H), 2.64 (s, 3H), 2.54 (s, 3H), 2.48 (m, 2H), 2.34 (s, 3H), 1.87 (m, 1H), 1.67 (ddd, J = 17.1, 13.1, 9.4 Hz, 1H), 1.37 (d, J = 6.7 Hz, 3H); m/z (ES+): 474 [M + H] ⁺ .

Example 108: Compound 108

(lS,8aS)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)- -methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)-carboxamide

To a solution of Intermediate 138 (220 mg, 0.36 mmol) in MeOH (5 mL) at 0 °C was added LiBH₄(16 mg, 0.72 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 2 h. After quenched with water, the resulting mixture was extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by Prep-HPLC to give the title compound (10 mg, yield: 5%). H NMR (400 MHz, CDCI₃) δ ppm 7.50 (s, 1H), 7.26 (m, 6H), 5.48 (d, J = 6.0 Hz, 1H), 4.13 (dd, J = 18.0, 11.7 Hz, 2H), 3.73 (ddd, J = 31.7, 29.7, 10.8 Hz, 5H), 3.37 (m, 4H), 2.66 (s, 3H), 2.55 (s, 3H), 1.88 (m, 1H), 1.66 (d, J = 6.2 Hz, 2H), 1.36 (d, J = 4.8 Hz, 3H); m/z (ES+): 554 [M + H] ⁺ .

Example 109: Compound 109

riS,8aS^')-/V-rrR^')-l-r3-ethyl-5-rtrifluoromethvnDhenvnethvn-/V-methyl-6-oxo-l-o- tolylhexahydropyrrolo[l,2-alpyrazine-2(l/-/)-carboxamide

To a solution of triphosgene (47 mg, 0.16 mmol) in EtOAc (2 mL) at 0 °C was added solution of ( lS,8aS)- l-o-tolylhexahydropyrrolo[ l,2-a] pyrazin-6(7H)-one (74 mg, 0.32 mmol), DMAP (4 mg, 0.032 mmol) and TEA (49 mg, 0.48 mmol) in EtOAc (2 mL) . The mixture was stirred for 1.5 h, followed by addition of (R)- l-(3-ethyl-5-(trifluoromethyl) phenyl)-N-methylethanamine ( 111 mg, 0.48 mmol) in EtOAc (2 mL) and TEA (97 mg, 0.963 mmol) . The reaction was stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc and the organic layer was washed with 1 M aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound (25 mg, yield : 17%) . ^JH NMR (400 MHz, CDCI₃) δ ppm 7.34 (s, 1 H), 7.26 (d, J = 7.8 Hz, 1 H), 7.20 (s, 1 H), 7.17 (d, J = 4.8 Hz, 1 H), 7.13 (dd, J = 14.9, 7.3 Hz, 2H), 7.06 (s, 1 H), 5.49 (q, J = 6.8 Hz, 1 H), 4.11 (dd, J = 20.6, 11.3 Hz, 2H), 3.71 (dd, J = 16.8, 7.4 Hz, 1 H), 3.28 (d, J = 11.9 Hz, 1 H), 3.11 (t, J = 12.3 Hz, 1H), 2.95 (td, J = 11.8, 2.9 Hz, 1 H), 2.66 (d, J = 10.2 Hz, 4H), 2.61 (d, J = 7.6 Hz, 1 H), 2.55 (s, 3H), 2.47 (m, 1 H), 2.38 - 2.26 (m, 1 H), 1.84 (ddd, J = 16.7, 13.0, 3.9 Hz, 1 H), 1.67 (ddd, J = 17.3, 13.1, 9.3 Hz, 1H), 1.36 (d, J = 6.6 Hz, 3H), 1.21 (t, J = 7.6 Hz, 3H) ; m/z (ES+) : 488 [M + H] ⁺ .

Exa mple 110 : Compound 110

riS,8aS^')-/V-rrR^')- l-r3-ethyl-5-rtrifluoromethvnphenvnethvn-7,7-bisr2-hvdroxyethvn-/V-

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 141 (78 mg, 0.14 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (76 mg, 1.98 mmol) . The reaction mixture was allowed to wa rm to room tempraure and stirred for 20 h. After quenched with water, the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then

concentrated in high vacuum . The residue was purified by Prep-HPLC to give the title compound (13 mg, yield: 16%). *H NMR (400 MHz, CDCI₃) δ ppm 7.34 (s, 1H), 7.25 (m, 5H), 7.04 (s, 1H), 7.25 (m, 1H), 5.50 (q, J = 6.8 Hz, 1H), 4.10 (m, 2H), 3.80 (m, 4H), 3.72 (m, 1H), 3.30 (d, J = 4.4 Hz, 1H), 3.12 (m, 1H), 3.00 (m, 1H), 2.70 (m, 5H), 2.54 (s, 3H), 1.84 (m, 7H), 1.35 (m, 2H), 1.20 (m, 3H); m/z (ES+): 576 [M + H] ⁺ .

Example 112: Compound 112

(lS,8aS)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- yrazine-2(l/-/)-carboxamide

To a solution of triphosgene (72 mg, 0.242 mmol) in EtOAc (5 mL) at 0 °C was added solution of (lS,8aS)-l-o-tolylhexahydropyrrolo[l,2-a]pyrazin-6(7/-/)-one (112 mg, 0.484 mmol), DMAP (6.2 mg, 0.05 mmol) and TEA (151 mg, 1.5 mmol) in EtOAc (15 mL). The mixture was stirred for 1.5 h, followed by addition of (R)-l-(3-isopropyl-5- (trifluoromethyl)phenyl)-/V-methylethanamine (142 mg, 0.58 mmol) in EtOAc (10 mL) and TEA (151 mg, 1.5 mmol). The reaction was then stirred at 50 °C for 48 h and quenched with water. The resulting mixture was extracted with EtOAc. The combined organic layer was washed with 1 N aqueous HCI solution, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum. The residue was purified by silica gel

chromatography (DCM/MeOH = 20/l to 10/1) to give the title compound (60 mg, yield: 25%) as yellow solid. ^JH-NMR (400 MHz, CDCI₃) δ ppm 7.37 (s, 1H), 7.27 (d, J = 6 Hz, 2H), 7.15 (m, 5H), 5.48 (m, 1H), 4.08 (m, 2H), 3.71 (m, 1H), 2.87 (m, 4H), 2.67 (s, 3H), 2.56 (s, 3H), 2.37(m, 2H), 1.82 (m, 1H), 1.64 (m, 1H), 1.35 (d, 3H), 1.22 (m, 3H); m/z (ES+): 502 [M + H] ⁺ . Example 113: Compound 113

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl) -/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(l/-/)-carboxamide

A slow stream of 0₃ in 0₂ was passed through a cooled solution of Intermediate 145 ( 100 mg, 0.172 mmol) in DCM ( 10 mL) at -78°C until a pale blue colour persisted . The reaction was purged with N₂ to remove the excess of 0₃ followed by addition of NaBH₄ (65 mg, 1.72 mmol) . The reaction mixture was allowed to wa rm to room tempraure and stirred for 20 h . The reaction was quenched with water and the resulting mixture was extracted with DCM . The organic layer was washed with brine, dried over anhydrous Na₂S0₄ and then concentrated in high vacuum . The residue was purified by Prep-HPLC to give the desired compound (20 mg, yield : 20%) . ^-NMR (400 MHz, CDCI₃) δ ppm 7.35 (s, 1 H), 7.26 (s, 2H), 7.10 (m, 5H), 5.46 (m, 1 H), 4.05 (m, 2H), 3.68 (m, 4H), 3.56 (m, 1 H), 2.85 (m, 4H), 2.65 (s, 3H), 2.55 (s, 3H), 1.66 (m, 7H), 1.33 (m, 3H), 1.20 (m, 3H) ; m/z (ES+) : 590 [M + H] ⁺ .

Exa mple 120

Measurement of NK1 receptor mediated intracellular [Ca²⁺1 mobilization in U251 MG cells using FLIPR

U251 MG cells were seeded into black walled clear-bottom 384-well plates (Greiner Bio- One GmbH, Frickenhausen, Germany) at a density of 15,000 cells/well in 50 μΙ culture medium and cultured overnight in a 37°C 5% C02 incubator. The cells were then loaded with the calcium sensitive dye Fluo-4 (Invitrogen) at 1 μΜ in buffer, containing 0.04% Pluronic F-127 (Sigma-Aldrich), and 2.5mM probenecid (Sigma-Aldrich) for 60 min in a humidified atmosphere of 5% C0₂. Thereafter, cells were washed three times in washing buffer containing 20mM H EPES and 2.5mM probenecid pH 7.3. Serial dilutions of test compounds in assay buffer containing 2% dimethyl sulfoxide (final concentration in the cell plate is 0.5% DMSO) and/or agonist were then automatically pipetted into each test well, and the peak fluorescence intensity was recorded (l_ex, 488 nm ; l_em, 540 nm) by the FLIPR instrument (Molecular Devices) for approximately 5 min . To measure antagonist potency, cell plates were first incubated with the test compound and intracellular fluorescence recorded for 5 minutes to check a potential agonist effect of the test compound . Cell plates were quickly removed from the FLIPR instrument and incubated for additional 10 minutes at 37°C before being moved back to the FLIPR instrument for Substance P (EC₈₀) addition . The response was measured as the pea k relative

fluorescence change after agonist addition . Compound relative %-effect was normalized to the maximal response evoked by ΙΟΟηΜ Aprepitant in presence of the EC₈o of Substance P and the antagonist potency

determined by non-linear regression using Gra phPad Prism (version 5) or the four- parameter logistic model in XL/it (IDBS, Guilford, UK) for Microsoft Excel (Microsoft, Redmond, WA). The IC50 value is defined as the molar concentration of a test compound that produces a response midway between the fitted top and the fitted bottom. pIC₅₀ = -logIC₅₀

Formula is listed as follows:

Fit (%Effect calculated) = (Α+((Β-Α)/(1+(^/Χ)^Λϋ))))

A: bottom value

B: top value

C: test compound concentration

X: Relative IC₅₀

D : Hill slope coefficient

Ref: Sullivan E, Tucker EM, and Dale IL. Measurement of [Ca²⁺] using the Fluorometric Imaging Plate Reader (FLIPR). Methods Mol Biol 114: 125-133, 1999.

Compounds of the present invention were tested according to example 120.

Results are reported in Table 1.

Example 121

Hepatic Extraction Ratio from Hepatic Intrinsic Clearance following incubation in human liver microsomes

The general procedure consists of an automated incubation system and LC-MS/MS analysis with human liver microsomes. Human liver microsomes are thawed rapidly in a waterbath at 37°C and kept on ice until use. The human liver microsomes are diluted with 50mM potassium phosphate buffer pH 7.4 to a protein concentration of 0.55mg/ml_. Test compounds and positive controls (Verapamil and Dextromethorphan, positive controls for CYP3A4 for CYP2D6 isoforms, respectively) are dissolved in methanol (or other appropriate solvent, if necessary) in order to obtain a 5mM solution which is further diluted to the concentration of 50μΜ. The stock solutions are prepared

immediately before the test.

5μΙ_ of 50μΜ test compounds and controls are added to 445 μΙ_-οί the 0.55mg/ml_ microsomes solution and the incubation mixture are pre-warmed at 37°C for 5 minutes. The incubation reactions are initiated by adding 50μΙ_ of pre-warmed NADPH

regenerating system to the incubation mixtures. ΞΟμί-ΒΜςυοίε will be taken from the incubation mixtures at: 0, 3, 6, 9, 15 and 30 minutes and the reactions are stopped by adding 100μΙ_ οί ACN containing Rolipram, used as generic Internal Standard (IS). Samples are then diluted with 120 μΙ_ of Mill i-Q water and centrifuged at 3000 rpm for 10 minutes, prior the LC-MS/MS analysis.

Intrinsic clearance.

The integrated peak areas for test compounds at the selected time points are divided by the respective peak areas of the IS and the percent of parent remaining is calculated by normalizing the peak area ratio of parent to IS at 0 min. Observed rate constant (k_obs) for parent degradation is calculated by determining the slope of the line of the graph of the natural log of percentage parent remaining versus time of incubation. From the rate of depletion (min-1) and volume of the incubation (ml_), clearance is estimated. This is scaled for the protein in the incubation relative to that in the intact liver, for all species (mL/min/g liver). imh incubation\ 52.5 mean mg protein

* ( 1 *

Clint = Rate / min \0.5 mg protein) g liver

Values for the Human in vitro Clint are expressed as mL/min/g liver.

Assuming a liver weight of 25.7 g/kg and a liver blood flow of 20.7 mL/min/kg, the hepatic extraction ratio, Eh, can be derived from the Human in vitro Clint:

{Clint * 25.7) * 20.7

E^{k =} {Clint * 25.7) + 20.7 ' ²° E.g. a Human in vitro Clint of 2.4 mL/min/g liver corresponds to a hepatic extraction ratio of 75%.

Some compounds of the present invention were tested according to example 121. Results are reported in Table 1 Table 1

ComU251MG Human in vitro

Name

pound (FLIPR Clint pIC₅₀) (mL/min/g liver)

N-[(3,5-dimethylphenyl)methyl]-N-methyl- l-(2-methylphenyl)-6-oxo-

8,19

octahydropyrrolo[ l,2- a]piperazine-2-ca rboxamide

N-[(3,5-dimethylphenyl)methyl]-N-methyl- l-(2-methylphenyl)-6-oxo-

7,U

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3-fluoro-5- trifluoromethyl) phenyl] methyl }-N-methyl- 1- (2-methylphenyl)-6-oxo- 8,86 9.5

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3-fluoro-5-

(trifluoromethy l)phenyl] methyl }-N-methy 1- l-(2-methylphenyl)-6-oxo- 7,09

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-methyl-l-(2-methylphenyl)-6-oxo-N-{[3- (trifluoromethy 1) phenyl] methyl }-

8,13

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-methyl-l-(2-methylphenyl)-6-oxo-N-{[3- (trifluoromethy 1) phenyl] methyl }-

<7

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-oxo-

8,97

octahydro-lH-pyrrolo[ l,2-a] [ l,4]diazepine- 2-ca rboxamide

2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c

arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 7,21

oxo-octahydropyrrolo[ l,2-a]piperazine-7- carboxylic acid

(!S,8aS)-N-[(lR)-l-[3,5- 10,46 4.5 bis(trifluoromethyl)phenyl]ethyl]-N-methyl- l-(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a] piperazine-2- ca rboxamide

(lR,8aR)-N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-N-methyl- l-(2-methylphenyl)-6-oxo- 7,89 octahydropyrrolo[ l,2-a] piperazine-2- ca rboxamide

Methyl 2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 9,09 oxo-octahydropyrrolo{l,2-a}piperazine-7- ca rboxylate

Methyl 2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 8,75 oxo-octahydropyrrolo{l,2-a}piperazine-7- ca rboxylate

Methyl 2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 8,38 oxo-octahydropyrrolo{l,2-a}piperazine-7- ca rboxylate

Methyl 2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 10,16 oxo-octahydropyrrolo{l,2-a}piperazine-7- ca rboxylate

Methyl 2-({[3,5- bis(trifluoromethyl) phenyl] methyl}(methyl)c arbamoyl)-7-methyl-l-(2-methylphenyl)-6- 10 oxo-octahydropyrrolo{l,2-a}piperazine-7- ca rboxylate

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

N-methyl-l-(2-methylphenyl)-6-oxo- 9,64 octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-6-oxo-

7,55

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

9,22 2.8 octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3,5-bis(trifluoromethyl)

phenyl] methyl}- 7-(hydroxymethyl)-N- methyl-l-(2-methyl phenyl) -6-oxo- 8,43

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3,5-bis(trifluoromethyl)

phenyl] methyl}- 7-(hydroxymethyl)-N- methyl-l-(2-methyl phenyl) -6-oxo- 8,78

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3,5-bis(trifluoromethyl)

phenyl] methyl}- 7-(hydroxymethyl)-N- methyl-l-(2-methyl phenyl) -6-oxo- 10,39

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3,5-bis(trifluoromethyl)

phenyl] methyl}- 7-(hydroxymethyl)-N- methyl-l-(2-methyl phenyl) -6-oxo- 10,29 0.8 octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{[3,5-bis(trifluoromethyl)

phenyl] methyl}- 7-(hydroxymethyl)-N- methyl-l-(2-methyl phenyl) -6-oxo- 10,11

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

N-methyl-l-(2-methylphenyl)- 8,87

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

2-N-{[3,5- bis(trifluoromethy 1) phenyl] methyl}-2-N, 7- N,7-N,7-tetramethyl- l-(2-methylphenyl)-6- 7,64

oxo-octahydropyrrolo[ l,2-a]piperazine-2,7- dica rboxamide

2-N-{[3,5- bis(trifluoromethyl) phenyl] methyl}-2-N, 7- N,7-N,7-tetramethyl- l-(2-methylphenyl)-6- 9,18 1.0 oxo-octahydropyrrolo[ l,2-a]piperazine-2,7- dica rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy lphenyl)-octa hyd ropy rrolo[ 1,2- 7,23

a]piperazine-2-ca rboxamide

methanesulfonic acid salt

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2- methy lphenyl)-octa hyd ropy rrolo[ 1,2- 9,04

a]piperazine-2-ca rboxamide

methanesulfonic acid salt

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin-

9,4 6.4 4-ylmethyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

N-methyl-l-(2-methylphenyl)-6-oxo-7-

(pyrrolidin-l-ylmethyl)- 9,42 2.4 octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

N-methyl-l-(2-methylphenyl)-6-oxo-7-

(pyrrolidin-l-ylmethyl)- 9,29

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

9,36

N-methyl-7-methylidene-l-(2- methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{l-[3,5-bis(trifluoromethyl)phenyl]-3- hydroxypropyl}-7-(2-hydroxyethyl)-N- methyl-l-(2-methylphenyl)-6-oxo- 9,8

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{l-[3,5-bis(trifluoromethyl)phenyl]-3- hydroxypropyl}-7-(2-hydroxyethyl)-N- methyl-l-(2-methylphenyl)-6-oxo- 7,81

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{l-[3,5-bis(trifluoromethyl)phenyl]-3- hydroxypropyl}-7-(2-hydroxyethyl)-N- methyl-l-(2-methylphenyl)-6-oxo- 9,7

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{l-[3,5-bis(trifluoromethyl)phenyl]-3- hydroxypropyl}-7-(2-hydroxyethyl)-N- methyl-l-(2-methylphenyl)- 9,14

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

7-[(4-acetylpiperazin-l-yl)methyl]-N-{[3,5- bis(trifluoromethy 1) phenyl] methy l}-N- methyl-l-(2-methylphenyl)-6-oxo- 9,51

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahyd ropy rrolo[ 1,2- 9,71 3.3 a]piperazine-2-ca rboxamide as

methansulfonic acid salt

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahydropyrrolo[ l,2- 8,54

a] pi perazine-2-ca rboxamide methansulfonic

acid salt N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahyd ropy rrolo[ 1,2- 8,11

a]piperazine-2-carboxamide methansulfonic

acid salt

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin- 4-ylmethyl)-6-oxa-octahyd ropy rrolo[ 1,2- 9,65 2.9 a]piperazine-2-carboxamide methansulfonic

acid salt

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- 7,7-bis(2-hydroxyethyl)-N-methyl-l-(2-

10,02

methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

9,28 3.7 methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

10,16 2.6 methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

(3'aS,4'S)-N-{[3,5- bis(trifluoromethyl) phenyl] methyl}-N, 1- d imethyl-4'-(2-methyl phenyl)- l'-oxo- 9,78 1.9 hexahydro-l'H-spiro[piperidine-4,2'- pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N,l-dimethyl-4'-(2-methylphenyl)-l'-oxo-

8,34

hexahydro-l'H-spiro[piperidine-4,2'- pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide

10,03 0.4 hexahydro-l'H-spiro[piperidine-4,2'- pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-

9,65

7-(hydroxymethyl)-N-methyl-l-(2- methyl phenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- 7-(hydroxymethyl)-N-methyl-l-(2-

9,46 1.9 methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-7-(morpholin-

9.65 2.9 4-ylmethyl)-6-oxa-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

9.92

4-ylmethyl)-6-oxa-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

9.29 3.1 methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]- 7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- 8.61

methylphenyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]- 7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- 9.92 9.5 methylphenyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7- (hydroxymethyl)-N-methyl-l-(2- 9.82 2.4 methylphenyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7-

9.95 0.34

(hydroxymethyl)-N-methyl-l-(2- methy lphenyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7-

(hydroxymethyl)-N-methyl-l-(2- 8.82

methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7-

(hydroxymethyl)-N-methyl-l-(2- 7.94

methy lphenyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]- 7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- 7.22

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]- 7,7-bis(2-hydroxyethyl)-N-methyl-l-(2- 9.47 6.1 methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-

<7

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}- N-methyl-l-(2-methylphenyl)-

9.02

octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-N-methyl-

9.49 11 1 -(2-methylphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-N-

7.37

methyl-l-(2-methylphenyl)- octahydropyrrolo[ l,2- a]piperazine-2-ca rboxamide

N-{[3,5- bis(trifluoromethy 1) phenyl] methyl}-7, 7- bis(2-hydroxyethyl)-N-methyl-l-(2- 7.52

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-{[3,5- bis(trifluoromethyl) phenyl] methyl}-7, 7- bis(2-hydroxyethyl)-N-methyl-l-(2- 10.1 4.2 methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7- (hydroxymethyl)-N-methyl-l-(2- 9.69

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7- (hydroxymethyl)-N-methyl-l-(2- 8.35

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7- (hydroxymethyl)-N-methyl-l-(2- 9.67

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-7- (hydroxymethyl)-N-methyl-l-(2- 7.18

methy lphenyl)-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-N- methyl-l-(2-methylphenyl)-7-(morpholin-4- 7.55

ylmethyl)-6-oxo-octa hyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- 8.09 bis(trifluoromethyl)phenyl]ethyl]-N- methyl-l-(2-methylphenyl)-7-(morpholin-4- ylmethyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- bis(trifluoromethyl)phenyl]ethyl]-N-

73 methyl-l-(2-methylphenyl)-7-(morpholin-4- 9.97

ylmethyl)-6-oxo-octahyd ropy rrolo[ 1,2- a]piperazine-2-ca rboxamide

N-[(lR)-l-[3,5- is(trifluoromethyl)phenyl]ethyl]-N-methyl-l-

74 (2-methylphenyl)-7-(morpholin-4-ylmethyl)- 10.05

6-oxo-octahydropyrrolo[ l,2-a]piperazine-2- ca rboxamide

/V-[(lR)-l-[3,5- is(trifluoromethyl)phenyl]ethyl]-/V-methyl-l-

75 (2-methylphenyl)-6-oxo- 10.5 32 octahydropyrrolo[ l,2-a] piperazine 2

ca rboxamide

(lS,8aS)-/V-(3-fluoro-5- (trifluoromethyl)benzyl)-7,7-bis(2-

76 hydroxyethyl)-/V-methyl-6-oxo-l-o- 9.83 12 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl- /V-(3-methyl-5-(trifluoromethyl)benzyl)-6-

77 10.2 15 oxo-l-o-tolylhexahydropyrrolo[ l,2- a]pyrazine-2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-(3- methoxy-5-(trifluoromethyl)benzyl)-/V-

78 methyl-6-oxo-l-o- 9.95 4.6 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-(3-chloro-5- (trifluoromethyl)benzyl)-7,7-bis(2-

79 9.98 14 hydroxyethyl)-/V-methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl- 6-oxo-l-o-tolyl-/V-(3-

80 9.33

(trifluoromethyl)benzyl)hexahydropyrrolo[ l,

2-a]pyrazine-2(l/-/)-ca rboxamide

(lS,8aS)-/V-(l-(3,5- bis(trifluoromethyl)phenyl)-3- hydroxypropyl)-7,7-bis(2-hydroxyethyl)-/V-

81 9.92

methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

82 9.95

methyl-6-oxo-l-o- tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

(lS,8aS)-/V-(l-(3,5- bis(trifluoromethy 1) phenyl) propyl)-7, 7-bis(2-

83 hydroxyethyl)-/V-methyl-6-oxo-l-o- 9.88 7.8 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl- /V-((S)-l-(3-methyl-5-

84 (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- 10.2 8.5 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl- /V-((R)-l-(3-methyl-5-

85 (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- 10.1 17 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((S)-l-(3,5- bis(trifluoromethyl)phenyl)-2-hydroxyethyl)-

86 7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l- 9.89 2.8 o-tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide (lS,8aS)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)-2-hydroxyethyl)-

87 7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l- 9.69

o-tolylhexahydropyrrolo[ l,2-a]pyrazine-

2(lH)-carboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl- 6-oxo-l-o-tolyl-/V-((R)-l-(3-

88 10.2 13

(trifluoromethyl)phenyl)ethyl)hexahydropyrr

olo[ l,2-a]pyrazine-2(l/-/)-carboxamide

(lS,8aS)-/V-((R)-l-(3-chloro-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

89 hydroxyethyl)-/V-methy 1-6-oxo- 1-o- 9.90 15 tolylhexahyd ropy rrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

(lS,8aS)-/V-((S)-l-(3-chloro-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

90 hydroxyethyl)-/V-methyl-6-oxo-l-o- 10.4 7.6 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l- (3-methoxy-5-

91 (trifluoromethyl)phenyl)ethyl)-/V-methy 1-6- 10.2 8.5 oxo- 1-o-tolylhexahyd ropy rrolo[ l, 2- a]pyrazine-2(l/-/)-ca rboxamide

(lS,8aS)-/V-((S)-l-(3-fluoro-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

92 hydroxyethyl)-/V-methy 1-6-oxo- 1-o- 10.8 11 tolylhexahyd ropy rrolo[ l,2-a] pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((R)-l-(3-fluoro-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

93 hydroxyethyl)-/V-methy 1-6-oxo- 1-o- 10.1 10 tolylhexahyd ropy rrolo[ l,2-a] pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((S)-l-(3-fluoro-5-

94 (trifluoromethyl)phenyl)-2-hydroxyethyl)- 10.3 3.4

7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l- o-tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methoxy- 5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

95 hydroxyethyl)-/V-methyl-6-oxo-l-o- 9.81 2.1 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((S)-2-hydroxy-l-(3- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

96 hydroxyethyl)-/V-methyl-6-oxo-l-o- 10.1 4.8 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((R)-l-(3-(difluoromethyl)-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

97 hydroxyethyl)-/V-methyl-6-oxo-l-o- 10.3 14 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

98 hydroxyethyl)-/V-methyl-6-oxo-l-o- 9.93 4.0 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((S)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

99 hydroxyethyl)-/V-methyl-6-oxo-l-o- 9.78 5.4 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamid

(l'S,8a'S)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-

100 6'-oxo-l'-o-tolylocta hydro- l'/-/-spiro[py ran- 9.90 3.0

4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'AV)- ca rboxamide

(l'S,8a'S)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-

101 6'-oxo-l'-o-tolylocta hydro- l'/-/-spiro[py ran- 10.6 6.9

4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'AV)- ca rboxamide (lS,8aS)-7-(hydroxymethyl)-/V-methyl-/V- ((R)-l-(3-methyl-5-

102 (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- 9.67 5.6 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-7,7-bis(hydroxymethyl)-/V-methyl- /V-((R)-l-(3-methyl-5-

103 (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- 10.1 4.8 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(lS,8aS)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-7,7-

104 bis(hydroxymethyl)-/V-methyl-6-oxo-l-o- 10.0 3.1 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

(l'S,8a'S)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-/V,l- d imethyl-6'-oxo-l'-o-tolyltetra hydro- l'H-

105 9.62 1.2 spiro[piperidine-4,7'-pyrrolo[ l,2- a]pyrazine]-2'(6'/-/)-ca rboxamide, formic

acid salt

(l'S,8a'S)-/V-((R)-l-(3,5- bis(trifluoromethyl)phenyl)ethyl)-/V-methyl- 6'-oxo-l'-o-tolyltetrahydro-l'AV-

106 9.94 0.19 spiro[piperidine-4,7'-pyrrolo[ l,2- alpyrazinel -2 '(6'H)-ca rboxamide, formic

acid salt

(lS,8aS)-/V-methyl-/V-((R)-l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-

107 9.97 9.2 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(lA7)-ca rboxamide

(lS,8aS)-/V-((R)-l-(3-chloro-5- (trifluoromethyl)phenyl)ethyl)-7,7-

108 bis(hydroxymethyl)-/V-methyl-6-oxo-l-o- 10.5 4.3 tolylhexahydropyrrolo[ l,2-a]pyrazine- 2(l/-/)-ca rboxamide

109 (lS,8aS)-/V-((R)-l-(3-ethyl-5- 10.0 13 (trifluoromethyl)phenyl)ethyl)-/V-methyl-6- oxo- l-o-tolylhexahyd ropy rrolo[ 1,2- a] pyrazine-2( l/-/)-ca rboxamide

( lS,8aS)-/V-((R)- l-(3-ethyl-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

110 hydroxyethyl)-/V-methyl-6-oxo- l-o- 10.2 13

tolylhexahydropyrrolo[ l,2-a] pyrazine- 2( l/-/)-ca rboxamide

( lS,8aS)-/V-((S)-2-hydroxy- l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-7,7-bis(2-

111 hydroxyethyl)-/V-methyl-6-oxo- l-o- 10.21 3.7

tolylhexahydropyrrolo[ l,2-a] pyrazine- 2( l/-/)-ca rboxamide

( lS,8aS)-/V-((R)- l-(3-isopropyl-5- (trifluoromethyl)phenyl)ethyl)-/V-methyl-6-

112 10.5 51

oxo- l-o-tolylhexahyd ropy rrolo[ 1,2- a] pyrazine-2( l/-/)-ca rboxamide

( lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)- l- (3-isopropyl-5-

113 (trifluoromethyl)phenyl)ethyl) -/V-methyl-6- 10.5 56

oxo- l-o-tolylhexahydropyrrolo[ l,2- a] pyrazine-2( l/-/)-ca rboxamide

Exa mple 122

Gerbil Scratching Model

Some compounds of the present invention were tested in the gerbil scratching model to evaluate the effect of the compounds in the scratching behavior induced in gerbil by administration of GR73632 (5-Aminopentanoyl-L-phenylalanyl-L-phenylalanyl-L-prolyl-L- (N-methyl)leucyl-L-methioninamide), a selective NK- 1 receptor agonist. The gerbil was selected for this study as this species shares higher homology to the human in terms of NK- 1 receptor pharmacology compared to other laboratory rodents.

Experimental procedure The day before the testing, animals (male Mongolian gerbils) were shaved on the rostral part of the back (approximately at the intrascapular level) to expose the skin around the area of GR73632 injection.

Each test compound was tested on 11 or 12 animals. On the day of the test, the gerbils (four animals simultaneously) were put into a Plexiglas cage (42 x 42 x 35 cm) composed of four cells (20.5 x 20.5 x 35 cm) for 10 minutes of habituation. After this period, the test compound (1% w/v in acetone and transcutol 9: 1) was topically applied on the shaven area in a volume of 20μΙ_. Topical application was performed using a Hamilton syringe (25 μΙ_) and a square stencil of impermeable paper (1.5 x 1.5 cm) to allow application over a defined skin area (2.25 cm2). After 20 minutes the animals received an intradermal (i.d.) injection of GR73632 (100 nmol/100 μΙ_ in NaCI 0.9%) in the centre of the pretreated area and were housed individually to prevent the animals from chafing each other's skin. I.d . injection was made with a Hamilton syringe (250 μΙ_) connected to a 27 gauge needle. Immediately after injection, animals were placed back into the same cell of the Plexiglas cage they were previously habituated in and their behaviour was recorded on video remotely for 30 minutes. The experimenter remained out of the observation room in order to minimize disturbance to the animals.

The video was subsequently analysed to assess scratching behaviour. Scratching of the injection site by the hind paws was counted while scratching of other sites such as ears and snout were disregarded. Scratching episodes were measured over 10-minutes time intervals, for a total of 30 minutes.

Results were expressed as mean value ± SEM. Statistical analysis was performed by a one-way ANOVA followed by LSD post hoc test with the exception of time-course analysis for a repeated-measure ANOVA followed by LSD post hoc test was performed.

Results

Figure 1 and Figure la shows that topical application of Compound 9 and Compound 44 were able to attenuate the scratching induced in gerbils by the NK-1 selective agonist (GR73632).

The time course of scratching behaviours over 30 minutes after the intradermal injection of GR73632 (100ηιηοΙ/100μί) is shown in Figure 1. The repeated-measure ANOVA showed that GR73632 induced an increase in the number of scratches [treat: F(l,3) = 15.36, p<0.001 ; time: F(l,2) =57.79, p<0.001 ; time x treat: F(l,6) = 10.30, p<0.001] . In particular, LSD ^' s post hoc analysis revealed a peaked effect of GR73632 within the first 10 minutes and this effect was maintained for the second 10-minute interval.

The effect of Compound 9 and Compound 44 during the first 10 minutes of the scratching model is shown in Figure la. One-way ANOVA analysis revealed a significant differences between treatment groups [F(l,3) = 13.33, p<0.001] . The post hoc test revealed a statistically significant effect for compound 9 (p<0.05) and compound 44 (p<0.001).

Figure 2 and figure 2a show that topical application of Compound 54 and Compound 60 was able to attenuate the scratching induced in gerbils by the NK-1 selective agonist (GR73632). The time course of scratching behaviours over 30 minutes after the intradermal injection of GR73632 (100ηιηοΙ/100μΙ_) is shown in Figure 2. The repeated-measure ANOVA statistical analysis showed that GR73632 induced an increase of scratching [treat: F(l,4) = 12.54, p<0.001 ; time: F(l,2) =80.77, p<0.001 ; time x treat: F(l,8) =5.58, p<0.001] . In particular, LSD post hoc analysis revealed a peak effect of GR73632 within the first 10 minutes which was maintained during the second 10-minute interval

The effect of Compound 54 and Compound 60 in during the first 10 minutes of the scratching model is shown in Figure 2a. One-way ANOVA analysis showed significant differences between treatment groups [F(l,4) =7.57, p<0.001] . The post hoc test revealed a statistically significant effect for compound 60 (p<0.01), compound 54 (p<0.01) and for the reference compound, Aprepitant (p<0.01).

Figure 3 and figure 3a shows that topical application of Compound 38 and Compound 55 was not able to attenuate the scratching induced in gerbils by the NK-1 selective agonist (GR73632)

The time course of scratching behaviour over 30 minutes after the intradermal injection of GR73632 (100ηιηοΙ/100μί) is shown in Figure 3. The repeated-measure ANOVA statistical analysis showed that GR73632 induced an increase of scratching [treat: F(l,3) =7.47, p<0.001 ; time: F(l,2) =79.22, p<0.001 ; time x treat: F(l,6) =6.47, p<0.001] . In particular, LSD post hoc analysis revealed a maximum effect of GR73632 within the first 10 minutes. The effect of Compound 38 and Compound 55 in the first 10 minutes of the scratching model is shown in Figure 3a. One-way ANOVA statistical analysis revealed significant differences between treatment groups [F(l,3) =7.43, p<0.001] . The post hoc test showed only a significant effect for induction of scratching behavior by GR73632 (p<0.001) compared to vehicle. However, neither Compound 38 nor Compound 55showed any statistically significant effect on reducing scratching behavior induced by GR73632.

Claims

1. A compound of general formula A

A

wherein

n is 1 or 2;

Rl and R2 are independently hydrogen, Ci_-4 alkyl, Ci_-4 haloalkyl, , Ci_-4 alkoxy, CD₃ or halogen ;

R5 and R6 are independently hydrogen, hydroxy, NR8R9, C(=0)R7, C(=0)OR7, C(=0)NR8R9, Ci-4 alkyl, wherein said Ci_-4 alkyl is optionally substituted with hydroxy, NR8R9 or a 5- or 6-membered heterocyclic ring, wherein said 5- or 6-membered heterocyclic ring is optiona lly substituted with Ci_-4 alkyl or C(=0)R7; or R5 and R6, together with the ca rbon atom to which they are attached, form =CH₂ or a 5- or 6- membered heterocycloalkyl, wherein said heterocycloa lkyl is optionally substituted with Ci-4 alkyl ;

R7 is hydrogen or Ci_-4 alkyl ;

R8 and R9 are independently hydrogen or Ci_-4 a lkyl, or R8 and R9, together with the nitrogen atom to which they are attached, form a 5- or 6-membered heterocyclic ring, or a pharmaceutically acceptable salt or solvate thereof.

2. A compound according to claim 1 of general formula A(i)

A(i)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated in clai

or a pharmaceutically acceptable salt or solvate thereof.

3. A compound according to claim 1 of general formula A(ii)

A(ii)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated in claim 1,

or a pharmaceutically acceptable salt or solvate thereof.

4. A compound according to any one of claims 1-3, wherein n is 1.

5. A compound according to any one of claims 1-4, wherein R4 is oxo.

6. A compound according to any one of claims 1-4, wherein R4 is hydrogen.

7. A compound according to any one of claims 1-6, wherein R3 is hydrogen, CH₃, CH₂CH₃, CH₂OH, CH₂CH₂OH, COOCH₃ or CH₂N(CH₃)₂.

8. A compound according to any one of claims 1-7, wherein R5 and R6 are both hydrogen.

9. A compound according to claims 1-7, wherein R5 is hydrogen, CH₃, CH₂OH or CH₂CH₂OH, and R6 is COOH, COOCH₃, CH₂OH, CH₂CH₂OH, CON(CH₃)₂ or CH₂- morpholine, CH₂-pyrrolidine, CH₂-piperazine optionally N-substituted with acetyl, or CH₂ piperidine.

10. A compound according to any one of claims 1-7, wherein R5 and R6, together with the carbon atom to which they are attached form =CH₂, a piperidine ring optionally substituted with Ci_-4 alkyl, or a tetrahydropyran ring.

11. A compound according to any one of claims 1-10 of general formula A(iii)

A(iii)

wherein n, Rl, R2, R3, R4, R5 and R6 are as indicated in claim 1,

or a pharmaceutically acceptable salt or solvate thereof.

12. A compound according to claim 11, wherein Rl is hydrogen, CH₃, fluoro or trifluoromethyl.

13. A compound according to claims 11 or 12, wherein R2 is hydrogen, chloro, CH₃, CH₂CH₃, isopropyl, OCH₃, difluoromethyl or trifluoromethyl.

14. A compound according to any one of claims 11-13, wherein Rl and R2 are both trifluoromethyl.

15. A compound according to any one of claims 11-13, wherein Rl is trifluoromethyl and R2 is methyl, ethyl or isopropyl.

16. A compound according to any one of claims 1-15 selected from the group consisting of

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N- [(3, 5-di methyl phenyl) methyl] -N-methy I- l-(2-methyl phenyl)-6-oxo- ctahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{[3-fluoro-5-(trifluoromethyl) phenyl] methyl }-N-methy 1-1 -(2-methylphenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-7-oxo- octahydro-lH-pyrrolo[ l,2-a] [ l,4]diazepine-2-carboxamide,

Methyl 2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carbamoyl)-7-methy I- 1-(2- methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a}piperazine-7-carboxylate,

Methyl 2-({ [3, 5-bis(trifluoromethyl) phenyl] methyl }(methyl)carbamoyl)-7-methy I- 1-(2- methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a}piperazine-7-carboxylate , N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)-6-oxo- octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-7-(hydroxymethyl)-N-methyl-l -(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide methanesulfonic acid salt,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-N-methyl-l-(2-methylphenyl)-7-(morpholi

4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-N-methyl-l -(2-methyl phenyl)-6-oxo-7-

(pyrrol id in-l-ylmethyl)-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-N-ethyl- l-(2-methyl pheny l)-6-oxo-7-

(pyrrol id in-l-ylmethyl)-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) pheny I] methyl }-N-methyl-7-methyl idene- 1-(2- methy I pheny l)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide, N-{1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethyl)-N-methyl- l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ 1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethy l)-N-methyl- l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-{ 1- [3, 5-bis(trifluoromethyl) phenyl] -3-hydroxy propyl }-7-(2-hydroxyethy l)-N-methyl- l-(2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

7- [(4-acetylpiperazin-l-yl) methyl] -N-{ [3, 5-bis(trifluoromethy I) phenyl] methyl }-N- methyl-l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-{ [3, 4-bis(trifluoromethyl) phenyl] methyl}-N-methyl-l-(2-methylphenyl)-7-(morpholin

4-ylmethyl)-6-oxa-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide as methansulfonic acid salt,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-7,7-bis(2-hydroxyethyl)-N-methy I- 1-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

(3'aS,4'S)-N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-N,l-dimethyl-4'-(2- methyl phenyl)- l'-oxo-hexa hydro- l'H-spiro[ pi peridine-4,2'-pyrrolo[ l,2-a] pi perazine] -5'- ca rboxamide,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N,l-d imethyl-4'-(2-methyl phenyl)- l'-oxo- hexa hydro- l'H-spiro[ pi peridine-4,2'-pyrrolo[ l,2-a]piperazine]-5'-ca rboxamide,

N-{[3,5-bis(trifluoromethyl)phenyl]methyl}-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide, N-{[3,5-bis(tnfluoromethyl)phenyl]methyl}-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l- (2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l-2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-6-oxo-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide ,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7,7-bis(2-hydroxyethyl)-N-methyl-l- (2-methylphenyl)-octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide ,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl}-N-methyl- l-(2-methyl phenyl)- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)- octahydropyrrolo[ l,2-a] pi perazine-2-ca rboxamide ,

N-{ [3, 5-bis(trifluoromethyl) phenyl] methyl }-7,7-bis(2-hydroxyethyl)-N-methy I- 1-(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide,

N-[(lR)-l-[3,5-bis(trifluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methy I phenyl)-octahyd ropy rrolo[ l,2-a] pi perazine-2-ca rboxamide, N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-7-(hydroxymethyl)-N-methyl-l-(2- methylphenyl)-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

N-[(lR)-l-[3,5-bis(tnfluoromethyl)phenyl]ethyl]-N-methyl-l-(2-methylphenyl)-7-

(morpholin-4-ylmethyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-2-carboxamide,

(lS,8aS)-/V-((S)-l-(3,5-bis(trifluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(l/-/)- ca rboxamide, (lS,8aS)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)-2-hydroxyethyl)-7,7-bis(2- hydroxyethyl)-/V-methy 1-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]py razine-2(lH)- ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-methyl-6-oxo-l-o-tolyl-/V-((R)-l-(3-

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-methoxy-5-

(lS,8aS)-/V-((S)-l-(3-fluoro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V methyl-6-oxo- 1-o-tolylhexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((S)-2-hydroxy-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2- hydroxyethyl)-/V-methyl-6-oxo-l-o-tolylhexahydropyrrolo[ l,2-a]pyrazine-2(l/-/)- ca rboxamide,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyloctahydro-l'/-/-spiro[pyran-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, (l'S,8a'S)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyloctahydro-l'/-/-spiro[pyran-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-carboxamide,

(lS,8aS)-7-(hydroxymethyl)-/V-methyl-/V-((R)-l-(3-methyl-5-

(trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(l/-/)- carboxamide ,

(lS,8aS)-7,7-bis(hydroxymethyl)-/V-methyl-/V-((R)-l-(3-methyl-5- (trifluoromethyl)phenyl)ethyl)-6-oxo-l-o-tolylhexahydropyrrolo[l,2-a]pyrazine-2(l/-/)- ca rboxamide,

(lS,8aS)-/V-((R)-l-(3,5-bis(tnfluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)-/V- methyl-6-oxo-l-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V,l-dimethyl-6'-oxo-l'-o- tolyltetrahydro-l'/-/-spiro[ pi peridine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, formic acid salt,

(l'S,8a'S)-/V-((R)-l-(3,5-bis(trifluoromethyl)phenyl)ethyl)-/V-methyl-6'-oxo-l'-o- tolyltetra hydro- l'/-/-spiro[ pi peridine-4,7'-pyrrolo[ l,2-a]pyrazine]-2'(6'/-/)-ca rboxamide, formic acid salt,

(lS,8aS)-/V-methyl-/V-((R)-l-(3-methyl-5-(trifluoromethyl)phenyl)ethyl)-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-chloro-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(hydroxymethyl)- /V-methyl-6-oxo-l-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-ethyl-5-(trifluoromethyl)phenyl)ethyl)-7,7-bis(2-hydroxyethyl)-/V- methyl-6-oxo-l-o-toly I hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl)-/V-methyl-6-oxo-l-o- tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide,

(lS,8aS)-7,7-bis(2-hydroxyethyl)-/V-((R)-l-(3-isopropyl-5-(trifluoromethyl)phenyl)ethyl) -/V-methyl-6-oxo-l-o-tolyl hexahyd ropy rrolo[ l,2-a]pyrazine-2(l/-/)-ca rboxamide or a pharmaceutically acceptable salt or solvate thereof.

17. A compound according to any one of claims 1-16 for use in therapy.

18. A compound according to claims 1-16 for use in the prevention, treatment or amelioration of pruritic skin conditions , e.g. acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurological or psychosomatic/psychiatric origin, including endocrine and metabolic disorders, infections, haematological and lymphoproliferative

diseases, solid neoplasms and drug-induced pruritus; mastocytosis; pruritus of unknown cause; pruritus with chronic secondary scratch lesions, such as prurigo nodularis, and all types of prurigo; or any other dermal disease or condition

characterized by pruritus.

19. The compound according to claim 18 wherein the pruritic skin condition is selected from prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, urticaria, mastocytosis and pruritus with chronic secondary scratch lesions.

20. A pharmaceutical composition comprising, as a therapeutically active ingredient, a compound according to any one of claims 1-16 and a pharmaceutically acceptable carrier or vehicle.

21. A pharmaceutical composition according to claim 20 together with one or more other therapeutically active compound(s).

22. A pharmaceutical composition according to claims 20-21 suitable for topical administration.

23. A method of preventing, treating or ameliorating a condition involving pruritus of the skin, the method comprising applying, on the skin of a patient in need thereof, a therapeutically effective amount of a compound according to any one of claims 1-16, optionally together with a pharmaceutically acceptable carrier or one or more excipients, optionally in combination with other therapeutically active compounds.

24. A method according to claim 23, wherein the condition is selected from the group consisting of acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurological or psychosomatic/psychiatric origin, including endocrine and metabolic disorders, infections, haematological and

25. The use of a compound according to claims 1-16 in the manufacture of a

medicament for the prevention, treatment or amelioration of pruritic skin conditions , e.g. acute pruritus in any condition; chronic pruritus on diseased skin, such as inflammatory, infectious, or autoimmune cutaneous diseases, genodermatoses, drug reactions, dermatoses of pregnancy and skin lymphomas, prurigo , lichen planus, atopic dermatitis, eczema, contact dermatitis, allergic dermatitis, nummular dermatitis, lichen simplex, psoriasis, Sezary syndrome, cutaneous lymphomas, bullous pemphigoid, alopecia areata, scabies, vitiligo, urticaria and drug-induced pruritus; pruritic diseases on non-diseased skin of systemic, neurological or psychosomatic/psychiatric origin, including endocrine and metabolic disorders, infections, haematological and

26. A compound according to general formula B

B

wherein RIO is selected from the group consisting of hydrogen and -C(0)OR14; Rl l is selected from the group consisting of hydrogen and oxo;

R12 and R13 are independently selected from the group consisting of hydrogen, C₁-C4 alkyl, allyl and -C(0)0(d-C₄ alkyl) ;

R14 is selected from the group consisting of Ci-C₄ alkyl;

n is 1 or 2;

or a pharmaceutically acceptable salt thereof.

27. The compound according to claim 26 selected from the group consisting of l-(2-methylphenyl)-octahydro-lH-pyrrolo[ l,2-a] [ l,4]diazepin-7-one;

1- (2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazin-6-one benzyl N-(2-{2-[(2- methylphenyl)carbonyl]-5-oxopyrrolidin-l-yl}ethyl)carbamate ;

tert-butyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo [ l,2-a]piperazine-2-carboxylate ;

2- tert-butyl 7-methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo [ 1,2-a] piperazine - 2,7 dicarboxylate;

(tert-butyl l-(2-methylphenyl)-6-oxohexahyd ropy rrolo[ 1,2-a] pyrazine-2(l/-/)- ca rboxylate);

Methyl 7-methyl-l-(2-methylphenyl)-6-oxo-octahydropyrrolo{ l,2-a} piperazine-7- ca rboxylate;

Methyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-7-carboxylate ; tert-butyl l-(2-methy I phenyl)-octahyd ropy rrolo[ 1,2-a] pi perazine-2-ca rboxylate;

l-(2-methy I phenyl)-octahyd ropy rrolo[ 1,2-a] piperazine;

l-(2-methylphenyl)-octahydropyrrolo[ l,2-a]piperazin-6-one hydrochloride salt; 2-tert- butyl 7,7-dimethyl l-(2-methylphenyl)-6-oxo-octahyd ropy rrolo[ 1,2-a] pi perazine-2, 7,7- trica rboxylate;

7,7-dimethyl l-(2-methylphenyl)-6-oxo-octahydropyrrolo[ l,2-a]piperazine-7,7- dica rboxylate;